Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_assertion description "[However, weak to absent GPx3 staining was observed in Barrett's dysplasia and adenocarcinoma samples where the promoter was hypermethylated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_assertion evidence source_evidence_literature NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_assertion SIO_000772 16229808 NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_assertion wasDerivedFrom befree-2016 NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_assertion wasGeneratedBy ECO_0000203 NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.
- befree-2016 importedOn "2016-02-19" NP518299.RArVCsS20siUUGCaM-ncy39IH5Dgtck3BMumY_nAs_HDw130_provenance.