http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#head http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#assertion http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#provenance http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#assertion http://rdf.disgenet.org/resource/gda/DGN845fff169144ce0ca50baa343ebe2dac http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/545 http://rdf.disgenet.org/resource/gda/DGN845fff169144ce0ca50baa343ebe2dac http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0025958 http://rdf.disgenet.org/resource/gda/DGN845fff169144ce0ca50baa343ebe2dac http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#provenance http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#assertion http://purl.org/dc/terms/description [Important insights into human neurogenesis are being revealed by the study of rare genetic diseases that involve primary microcephaly, illustrated by the identification of the Microcephalin, abnormal spindle in microcephaly and ataxia-telangiectasia and Rad3-related genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#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/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/15018946 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#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/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/dc/terms/created 2017-10-17T13:10:48+02:00 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP95622.RAf8rfIPxFaXvswRMoDC5zn2cI94ZUswdexYVF3eNbRK0 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