@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:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_head { this: np:hasAssertion dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_assertion; np:hasProvenance dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_provenance; np:hasPublicationInfo dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_publicationInfo; a np:Nanopublication . dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_assertion a np:Assertion . dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_provenance a np:Provenance . dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_publicationInfo a np:PublicationInfo . } dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_assertion { miriam-gene:4893 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGNf73660485645f62d5c2a15c324f5ecc6 sio:SIO_000628 miriam-gene:4893, lld:C0025202; a sio:SIO_001122 . } dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_provenance { dgn-np:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_assertion dcterms:description "[In this study, we performed an integrative analysis of DNA methylation, gene expression, and microRNA expression data to identify potential regulatory pathways associated with the most common driver mutations in NRAS (Q61K/L/R) through comparison of NRASQ61-mutated melanomas with pan-negative 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:25537510; 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:NP1250940.RAoBGFwd4sJbCjldUhKifwpWPjvt5eXPgDH-PLBhHyVug130_publicationInfo { this: dcterms:created "2016-05-13T12:51:13+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" . }