Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- befree-2016 importedOn "2016-02-19" NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_assertion wasGeneratedBy ECO_0000203 NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_assertion wasDerivedFrom befree-2016 NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_assertion SIO_000772 17728257 NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_assertion evidence source_evidence_literature NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.
- NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_assertion description "[Because of their high sequence homology, the missense mutations in MMAA that result in methylmalonic aciduria have been mapped onto MeaB and, in conjunction with mutagenesis data, provide possible explanations for the pathology of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627228.RAAlsFRlte4hG1rTtxX7kvOuvDnTkMNNqSIJFuOIXUWvI130_provenance.