@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:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_head { this: np:hasAssertion dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_assertion; np:hasProvenance dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_provenance; np:hasPublicationInfo dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_publicationInfo; a np:Nanopublication . dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_assertion a np:Assertion . dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_provenance a np:Provenance . dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_publicationInfo a np:PublicationInfo . } dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_assertion { miriam-gene:1029 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGNadb47f4782fbe6a4415f3c9bede44ac6 sio:SIO_000628 miriam-gene:1029, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_provenance { dgn-np:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_assertion dcterms:description "[Our results, obtained in a heterogeneous group of families, support the view that inactivating mutations of CDKN2A contribute to melanoma susceptibility more than activating mutations of CDK4 and that other genetic factors must be responsible for melanoma clustering in a high proportion of families.]. 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:11556834; 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:NP330149.RATbIfbQgBxHxj4z0-2wSSeYfIMoNLv6ucf1xoO1YImrA130_publicationInfo { this: dcterms:created "2016-05-13T12:44:15+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" . }