@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:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_head { this: np:hasAssertion dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_assertion; np:hasProvenance dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_provenance; np:hasPublicationInfo dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_publicationInfo; a np:Nanopublication . dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_assertion a np:Assertion . dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_provenance a np:Provenance . dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_publicationInfo a np:PublicationInfo . } dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_assertion { miriam-gene:1956 a ncit:C16612 . lld:C0009402 a ncit:C7057 . dgn-gda:DGN96797a19e22d733f1b8e685f4dbce897 sio:SIO_000628 miriam-gene:1956, lld:C0009402; a sio:SIO_001121 . } dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_provenance { dgn-np:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_assertion dcterms:description "[Our results suggest that standard cytology provides adequate material for the assessment of EGFR and Kras mutational status in NSCLC and CRC patients and could be specifically indicated in patients not eligible for surgery but candidate to anti-EGFR therapy.]. 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:22833420; 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:NP1000448.RAPjVWaTmjNHT3vYTLZmy42cuN5wfXPMj5nbFnuNfbx8s130_publicationInfo { this: dcterms:created "2016-05-13T12:49:19+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }