@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_head { this: np:hasAssertion dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_assertion; np:hasProvenance dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_provenance; np:hasPublicationInfo dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_publicationInfo; a np:Nanopublication . dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_assertion a np:Assertion . dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_provenance a np:Provenance . dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_publicationInfo a np:PublicationInfo . } dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_assertion { miriam-gene:6310 a ncit:C16612 . lld:C0024408 a ncit:C7057 . dgn-gda:DGN126e6bea39dbfe378bab279fff5c5042 sio:SIO_000628 miriam-gene:6310, lld:C0024408; a sio:SIO_001121 . } dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_provenance { dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_assertion dcterms:description "[They include at least nine disorders, including Huntington's disease (HD), dentatorubral pallidoluysian atrophy (DRPLA), spinal and bulbar muscular atrophy (SBMA), and the spinocerebellar ataxias SCA1, SCA2, SCA3 (also known as Machado-Joseph disease), SCA6, SCA7, and SCA17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:17786457; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP628462.RA9XHqlkFkYWCIHAP00_JOONFpur2pGVHClxvUQwtp1rw130_publicationInfo { this: dcterms:created "2016-05-13T12:46:30+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }