Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_assertion description "[Here we report the isolation and sequencing of the human gene encoding malonyl CoA decarboxylase, and the identification of a mutation causing malonyl CoA decarboxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_assertion evidence source_evidence_literature NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_assertion SIO_000772 9869665 NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_assertion wasDerivedFrom befree-2016 NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_assertion wasGeneratedBy ECO_0000203 NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411946.RAbh2OzmU0r8vPKO5aJ2vxL1a7TFA65LweS01VBHT42s8130_provenance.