Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_assertion description "[The copy number variation of erbB2 gene from plasma can be used as prognostic marker for early detection of patients at risk of worse clinical outcome in esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_assertion evidence source_evidence_literature NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_assertion SIO_000772 21481261 NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_assertion wasDerivedFrom befree-20150227 NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_assertion wasGeneratedBy ECO_0000203 NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP379855.RAyhkMYCtYF0hPt0tuq3N3Du0dcpVdJcs7aKaIqZ8195U130_provenance.