@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:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_head { this: np:hasAssertion dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_assertion; np:hasProvenance dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_provenance; np:hasPublicationInfo dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_publicationInfo; a np:Nanopublication . dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_assertion a np:Assertion . dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_provenance a np:Provenance . dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_publicationInfo a np:PublicationInfo . } dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_assertion { miriam-gene:238 a ncit:C16612 . lld:C0007131 a ncit:C7057 . dgn-gda:DGN286180e76f23b92564ad2f4aa0cba8de sio:SIO_000628 miriam-gene:238, lld:C0007131; a sio:SIO_001121 . } dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_provenance { dgn-np:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_assertion dcterms:description "[The frequencies of EGFR mutation and ALK translocation in the study cohort are greater than the reported frequencies among NSCLC from adults of all ages in the United States but less than the reported frequencies among NSCLC from East Asian young adults.]. 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:25288236; 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:NP1226783.RASX2EBgg_Yqd_4q4NgQQUxN49Kv0eRfAS2UfFvnAn9ME130_publicationInfo { this: dcterms:created "2016-05-13T12:51:02+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" . }