@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:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_head { this: np:hasAssertion dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_assertion; np:hasProvenance dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_provenance; np:hasPublicationInfo dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_publicationInfo; a np:Nanopublication . dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_assertion a np:Assertion . dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_provenance a np:Provenance . dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_assertion { miriam-gene:6098 a ncit:C16612 . lld:C0007131 a ncit:C7057 . dgn-gda:DGN59cbd3a73b87ac0cf6ab9be6df305e36 sio:SIO_000628 miriam-gene:6098, lld:C0007131; a sio:SIO_001121 . } dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_provenance { dgn-np:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_assertion dcterms:description "[TMEM106B-ROS1 is a novel ROS1 fusion variant in NSCLC identified by comprehensive genomic profiling and should be included in any ROS1 detecting assay that depends on identifying the corresponding fusion partners such as reverse transcriptase-polymerase chain reaction (RT-PCR).]. 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:25851827; 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:NP1276457.RAYRJSTjNHCkJDq-G4I1rlSPnx9ogERK0YS2uCx4obveU130_publicationInfo { this: dcterms:created "2016-05-13T12:51:24+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" . }