Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_assertion description "[Methionine synthase reductase (MSR) deficiency is an autosomal recessive disorder of folate/cobalamin metabolism leading to hyperhomocysteinemia, hypo- methioninemia and megaloblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_assertion evidence source_evidence_literature NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_assertion SIO_000772 10484769 NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_assertion wasDerivedFrom befree-2016 NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_assertion wasGeneratedBy ECO_0000203 NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.
- befree-2016 importedOn "2016-02-19" NP262843.RAfllvtujtix_EFaRneQL2LzA1duvFNauuss0aBR8hg0E130_provenance.