@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:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_head { this: np:hasAssertion dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_assertion; np:hasProvenance dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_provenance; np:hasPublicationInfo dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_publicationInfo; a np:Nanopublication . dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_assertion a np:Assertion . dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_provenance a np:Provenance . dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_publicationInfo a np:PublicationInfo . } dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_assertion { miriam-gene:79811 a ncit:C16612 . lld:C0007137 a ncit:C7057 . dgn-gda:DGNd8b45692304a32faefa7f0843c315e22 sio:SIO_000628 miriam-gene:79811, lld:C0007137; a sio:SIO_001121 . } dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_provenance { dgn-np:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_assertion dcterms:description "[Recent research is revealing combinations of disturbed oncogenic and tumor-suppressive signaling pathways by altered or missing genes in skin cancers: mutated PTCH (in the mitogenic Sonic Hedgehog pathway) and mutated p53 tumor suppressor gene in basal cell carcinomas (BCC), possibly an activated mitogenic RAS pathway and mutated p53 in squamous cell carcinomas (SCC), and possibly an activated MET/RAS pathway and inactive p16(INK4a) tumor suppressor in cutaneous melanomas.]. 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:12239425; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP945753.RAg1XBYnRjRTynXfiHzJ6f4lzrOiFDLXOM4FeLa5B44mI130_publicationInfo { this: dcterms:created "2015-08-25T14:47:17+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }