Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion description "[As there is increasing evidence that CENPF is associated with poor prognosis in patients with primary BC, further independent studies are needed to clarify the importance of genetic variation in the CENPF gene in the clinic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion evidence source_evidence_literature NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion SIO_000772 19008095 NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion wasDerivedFrom befree-20140225 NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion wasGeneratedBy ECO_0000203 NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance.