Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_assertion description "[We have identified the mutation in a phosphoglycerate kinase variant (PGK-Matsue) associated with severe enzyme deficiency, congenital nonspherocytic hemolytic anemia, and mental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_assertion evidence source_evidence_literature NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_assertion SIO_000772 2001457 NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_assertion wasDerivedFrom befree-20150227 NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_assertion wasGeneratedBy ECO_0000203 NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP643748.RA8mjNGhNwp3wVGDwtN_TfNvYy3QOOL7QZR09uULofjvk130_provenance.