@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:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_head { this: np:hasAssertion dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_assertion; np:hasProvenance dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_provenance; np:hasPublicationInfo dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_publicationInfo; a np:Nanopublication . dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_assertion a np:Assertion . dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_provenance a np:Provenance . dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_publicationInfo a np:PublicationInfo . } dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_assertion { miriam-gene:1956 a ncit:C16612 . lld:C0684249 a ncit:C7057 . dgn-gda:DGNd49b9b495756c4f3cda6ddbe16ca9cde sio:SIO_000628 miriam-gene:1956, lld:C0684249; a sio:SIO_001121 . } dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_provenance { dgn-np:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_assertion dcterms:description "[The most widely used types of molecular analysis in routine cellular pathology are EGFR testing in lung cancer, molecular testing of thyroid nodules, fluorescence in situ hybridization testing of urine samples, clonality analysis in lymphoma testing, HER2 testing in breast and gastric cancer, KRAS testing in colorectal cancer, intraoperative assessment of breast cancer sentinel nodes, molecular testing of gastrointestinal stromal tumours and mismatch repair protein analysis.]. 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:22846108; 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:NP1001406.RA6rEwkoDzNko3COhi_78BIXiS22LGXQgfLcf_DD77zMA130_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" . }