Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_assertion description "[Several other genetic regions including variants of CHEK2 (22q12), TP53BP1 (15q15) and RAD52 (12p13) have been demonstrated to influence lung cancer risk in candidate- or pathway-based analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_assertion evidence source_evidence_literature NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_assertion SIO_000772 22899653 NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_assertion wasDerivedFrom befree-2016 NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_assertion wasGeneratedBy ECO_0000203 NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1005883.RAnUamft9FkEB5MgusnaArLGobGzY6HexfcA2vEVzQQwQ130_provenance.