Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_assertion description "[Alterations of the human MSH2 gene, a homologue of the bacterial MutS mismatch repair gene, co-segregate with the majority of hereditary non-polyposis colon cancer (HNPCC) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_assertion evidence source_evidence_literature NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_assertion SIO_000772 7550317 NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_assertion wasDerivedFrom befree-2016 NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_assertion wasGeneratedBy ECO_0000203 NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1312168.RAuNZLH2P4LThVKCxH2gwE40xumQEvRdZXtnM9VzsIpu0130_provenance.