Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_assertion description "[We evaluated a series of European CRC patients and population controls to clarify whether EXO1 variants may indeed predispose to familial CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_assertion evidence source_evidence_literature NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_assertion SIO_000772 12517792 NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_assertion wasDerivedFrom befree-2016 NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_assertion wasGeneratedBy ECO_0000203 NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.
- befree-2016 importedOn "2016-02-19" NP379606.RA8pYGuwOlJ4Zsz0OWugrYnORw0_Hb17Wck528dqf92LI130_provenance.