Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_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." NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_assertion evidence source_evidence_literature NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_assertion SIO_000772 12068375 NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_assertion wasDerivedFrom befree-20140225 NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_assertion wasGeneratedBy ECO_0000203 NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.