Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_assertion description "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_assertion evidence source_evidence_literature NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_assertion SIO_000772 12068375 NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_assertion wasDerivedFrom befree-2016 NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_assertion wasGeneratedBy ECO_0000203 NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.
- befree-2016 importedOn "2016-02-19" NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.