Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_assertion description "[The mean concentration of FIXP was markedly reduced to 22.7 pmol/L in nine patients with hereditary factor VII deficiency (factor VII coagulant activity less than 7%) but was not significantly different from normal controls in nine subjects with factor XI deficiency (factor XI coagulant activity less than 8%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_assertion evidence source_evidence_literature NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_assertion SIO_000772 2383653 NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_assertion wasDerivedFrom befree-20140225 NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_assertion wasGeneratedBy ECO_0000203 NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP597060.RAlpTVwS_0TRds1ml6gb4kMJgpl0Dri0bfDRCICcD5OHE130_provenance.