Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- befree-2016 importedOn "2016-02-19" NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_assertion wasGeneratedBy ECO_0000203 NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_assertion wasDerivedFrom befree-2016 NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_assertion SIO_000772 20533283 NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_assertion evidence source_evidence_literature NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.
- NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_assertion description "[We verified that the frequency of MSI was similar in familial and sporadic GC settings, demonstrating that this molecular phenotype is not a hallmark of familial GC in contrast to what is verified in HNPCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817425.RAR3Vw_BmGgss98t3OjgyIjIaDMwJaxg_DuhyhJr7s0l0130_provenance.