Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_assertion description "[The cblD defect of intracellular vitamin B(12) metabolism can lead to isolated methylmalonic aciduria (cblD-MMA) or homocystinuria (cblD-HC), or combined methylmalonic aciduria and homocystinuria (cblD-MMA/HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_assertion evidence source_evidence_literature NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_assertion SIO_000772 22156578 NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_assertion wasDerivedFrom befree-20140225 NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_assertion wasGeneratedBy ECO_0000203 NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP211702.RAc1iUs2PRH5MeAB_vER_-0YUjhY4YtGWrFlZVfTPjKlc130_provenance.