Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_assertion description "[Fascin increased across the following states as follows: normal-appearing epithelium (26%) to dysplasia (46%) to ESCC (68%), while CK4 was undetectable in ESCC (0%) compared to normal-appearing epithelium (45%) or dysplasia (41%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_assertion evidence source_evidence_literature NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_assertion SIO_000772 21498718 NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_assertion wasDerivedFrom befree-20140225 NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_assertion wasGeneratedBy ECO_0000203 NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401298.RAv3urrFfug3-e69-HOnHMWDySeDf-deZgK39T9mO66NM130_provenance.