Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_assertion description "[Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_assertion evidence source_evidence_literature NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_assertion SIO_000772 8765219 NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_assertion wasDerivedFrom befree-2016 NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_assertion wasGeneratedBy ECO_0000203 NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1355856.RAz6-Swdnpd8vgzpnm7heKLecSzDNho3TYjtqn3e1AZNY130_provenance.