http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#head
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#assertion
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#provenance
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#assertion
http://rdf.disgenet.org/resource/gda/DGN3c8977931e149cf4eb929233fbeb6b6b
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/3064
http://rdf.disgenet.org/resource/gda/DGN3c8977931e149cf4eb929233fbeb6b6b
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0020179
http://rdf.disgenet.org/resource/gda/DGN3c8977931e149cf4eb929233fbeb6b6b
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#provenance
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#assertion
http://purl.org/dc/terms/description
[The results further support the evidence that the repeat expansion at the chromosome 16q24.3 locus is the direct cause of HDL2 and provide preliminary guidelines for the genetic testing of patients with an HD-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#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/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/15468075
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/GAD
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/GAD
http://purl.org/pav/importedOn
2017-02-21
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/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/dc/terms/created
2017-10-17T13:13:14+02:00
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP480133.RAqCPuT2_hdBDl9LXOYdF576LAlMaKrtzF01aS6VAKGjA
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