Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_assertion description "[Mutations in the MMAA gene on human chromosome 4q31.21 result in vitamin B12-responsive methylmalonic aciduria (cblA complementation group) due to deficiency in the synthesis of adenosylcobalamin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_assertion evidence source_evidence_literature NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_assertion SIO_000772 15523652 NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_assertion wasDerivedFrom befree-20140225 NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_assertion wasGeneratedBy ECO_0000203 NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP909782.RAI0UTsDpwYOX59Eb6LazZNuD1SKYvoqW2omI2-_Sl6IY130_provenance.