Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_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." NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_assertion evidence source_evidence_literature NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_assertion SIO_000772 19755962 NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_assertion wasDerivedFrom befree-20150227 NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_assertion wasGeneratedBy ECO_0000203 NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP627049.RA5to_3jY9cJlSF-0Sia7IjVEdNimhR-Jl3qV75mfD_cw130_provenance.