Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion description "[Prothrombin deficiency is a rare (1:200 000) autosomal recessive disorder caused by diverse mutations in prothrombin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion evidence source_evidence_literature NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion SIO_000772 15892853 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion wasDerivedFrom befree-20140225 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion wasGeneratedBy ECO_0000203 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.