Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_assertion wasGeneratedBy ECO_0000203 NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_assertion wasDerivedFrom befree-20150227 NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_assertion SIO_000772 8575782 NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_assertion evidence source_evidence_literature NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.
- NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_assertion description "[Defect of GPI biosynthesis due to somatic mutation in the hematopoietic stem cell is the basis for an acquired genetic disease, paroxysmal nocturnal hemoglobinuria (PNH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431113.RAnpfFkeVPrVxyArJRVZzoAnBg0yEM1p55welL8CDbnBk130_provenance.