@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:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_head { this: np:hasAssertion dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_assertion; np:hasProvenance dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_provenance; np:hasPublicationInfo dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_publicationInfo; a np:Nanopublication . dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_assertion a np:Assertion . dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_provenance a np:Provenance . dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_publicationInfo a np:PublicationInfo . } dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_assertion { miriam-gene:238 a ncit:C16612 . lld:C1516669 a ncit:C7057 . dgn-gda:DGNdea157c6b77761796185d205e82ca620 sio:SIO_000628 miriam-gene:238, lld:C1516669; a sio:SIO_001121 . } dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_provenance { dgn-np:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_assertion dcterms:description "[Whether the rare expression of NPM/ALK is the result of clonal heterogeneity or an indication for clonal evolution and progression toward ALCL can only be answered by the repeated analysis of indicator cases during the course of the disease.]. 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:9209648; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP235843.RAZND7acSlIy-De3jIvt9ioYxn2JrEhQ3yqRLw_v6Vhtc130_publicationInfo { this: dcterms:created "2015-08-25T14:39:54+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }