@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:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_head { this: np:hasAssertion dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_assertion; np:hasProvenance dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_provenance; np:hasPublicationInfo dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_publicationInfo; a np:Nanopublication . dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_assertion a np:Assertion . dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_provenance a np:Provenance . dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_assertion { miriam-gene:238 a ncit:C16612 . lld:C1527249 a ncit:C7057 . dgn-gda:DGNaf579e6dd66d3b3bffd459817b6ddcfe sio:SIO_000628 miriam-gene:238, lld:C1527249; a sio:SIO_001121 . } dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_provenance { dgn-np:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_assertion dcterms:description "[Here, we summarize the clinically relevant biomarker tests that should be considered in neurosurgical specimens based on the current recommendations of the European Society of Medical Oncology (ESMO) or the National Comprehensive Cancer Network (NCCN) for the most relevant primary tumor types: lung cancer (EGFR mutations, ALK rearrangement, BRAF mutations), breast cancer (HER2 amplification, steroid receptor overexpression), melanoma (BRAF mutations), and colorectal cancer (RAS mutations).]. 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:25287912; 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:NP1226738.RA51Xnq2iOA7ODWHWEfu51W-zsR5uF2Hc1LFkqp6UWucY130_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" . }