http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#head http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#provenance http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://rdf.disgenet.org/resource/gda/DGN43176f63b76aef7e04740d51f580ecba http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/3897 http://rdf.disgenet.org/resource/gda/DGN43176f63b76aef7e04740d51f580ecba http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0025362 http://rdf.disgenet.org/resource/gda/DGN43176f63b76aef7e04740d51f580ecba http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#provenance http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://purl.org/dc/terms/description [Hereditary spastic paraplegias (HSP), a group of genetically heterogeneous neurological disorders with more than 56 documented loci (SPG1-56), are described either as uncomplicated (or pure), or complicated where in addition to spasticity and weakness of lower extremeties, additional neurological symptoms are present, including dementia, loss of vision, epilepsy, mental retardation and ichthyosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/26113134 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/dc/terms/created 2017-10-17T13:14:13+02:00 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP632852.RAOiPie419IM9vsfKXkGqcGcT2ARCgVkI1NYMgT6Ns86M http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0