@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:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_head { this: np:hasAssertion dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion; np:hasProvenance dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_provenance; np:hasPublicationInfo dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_publicationInfo; a np:Nanopublication . dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion a np:Assertion . dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_provenance a np:Provenance . dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_publicationInfo a np:PublicationInfo . } dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion { miriam-gene:7428 a ncit:C16612 . lld:C0019562 a ncit:C7057 . dgn-gda:DGNc78462e6764d8fdfdc41fcb0581d49dd sio:SIO_000628 miriam-gene:7428, lld:C0019562; a sio:SIO_001121 . } dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_provenance { dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion dcterms:description "[von Hippel-Lindau (VHL) disease is an autosomal dominant inherited tumor syndrome characterized by the development of tumors in the eye, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis, associated with germline mutations in the VHL gene.]. 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:19270817; 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:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_publicationInfo { this: dcterms:created "2016-05-13T12:47:13+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" . }