Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_assertion description "[In newborns with homozygous protein C deficiency with very low protein C levels (1%) a purpura fulminans like syndrome was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_assertion evidence source_evidence_literature NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_assertion SIO_000772 3524711 NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_assertion wasDerivedFrom befree-20140225 NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_assertion wasGeneratedBy ECO_0000203 NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP464397.RAdI5d5gIzs9xUEhwh6k_XVgMGV9NGP1T7HID3woN0ACk130_provenance.