Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_assertion description "[Human erythrocyte R-type pyruvate kinase deficiency (PKD) is a disorder caused by mutations in the PKLR gene that produces chronic nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_assertion evidence source_evidence_literature NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_assertion SIO_000772 19755962 NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_assertion wasDerivedFrom befree-20140225 NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_assertion wasGeneratedBy ECO_0000203 NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171046.RAbVt_7Qf367CjhnzDAKpFdJnaD-5v8HGKtOrF5Gu0hKI130_provenance.