@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:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_head { this: np:hasAssertion dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_assertion; np:hasProvenance dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_provenance; np:hasPublicationInfo dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_publicationInfo; a np:Nanopublication . dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_assertion a np:Assertion . dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_provenance a np:Provenance . dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_assertion { miriam-gene:5900 a ncit:C16612 . lld:C1306459 a ncit:C7057 . dgn-gda:DGNc257af9553adc3eade4fc3eee54ef64d sio:SIO_000628 miriam-gene:5900, lld:C1306459; a sio:SIO_001121 . } dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_provenance { dgn-np:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_assertion dcterms:description "[An example is RAS, which is frequently mutated in cancer and contributes to initiation and maintenance of the disease by constitutive signal transduction through protein interaction with effector proteins, like PI3K, RAF and RALGDS.]. 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:17568777; 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:NP665013.RAkP76EGTH1T1ow1ebIvOHrc-6Rd8CmAZwaqAEsb8MNvQ130_publicationInfo { this: dcterms:created "2015-08-25T14:44:19+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" . }