Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_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." NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_assertion evidence source_evidence_literature NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_assertion SIO_000772 9869665 NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_assertion wasDerivedFrom befree-20150227 NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_assertion wasGeneratedBy ECO_0000203 NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872520.RAtkL407VtBXU1I9zicQw4vUQoSLXZ3SNX0CEOIbecYSI130_provenance.