Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_assertion description "[A recent report proposed two missense mutations (c.1032C-->A and c.1032C-->G) in F12, the gene encoding human coagulation factor XII (FXII, or Hageman factor) as a possible cause of HAE type III.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_assertion evidence source_evidence_literature NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_assertion SIO_000772 17186468 NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_assertion wasDerivedFrom befree-20150227 NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_assertion wasGeneratedBy ECO_0000203 NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392830.RAiZpLTI2sTWwoZEHQQJYTa1j_FWp_GGh_BU19ZgJybaY130_provenance.