Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_assertion description "[Biopsy specimens from patients with inactive UC (n=18), active UC (n=28), UC with low-grade dysplasia (LGD) (n=9), UC with high-grade dysplasia (HGD) (n=7), UC-CRC (n=11) and sporadic CRC (n=14) were included.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_assertion evidence source_evidence_literature NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_assertion SIO_000772 19926618 NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_assertion wasDerivedFrom befree-20140225 NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_assertion wasGeneratedBy ECO_0000203 NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP358983.RAKklZZ92l0NgAbemOYIdGKFMGXcGGKJxW4Xw975y_2LE130_provenance.