Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_assertion description "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_assertion evidence source_evidence_literature NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_assertion SIO_000772 22951388 NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_assertion wasDerivedFrom befree-20140225 NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_assertion wasGeneratedBy ECO_0000203 NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.