Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_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." NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_assertion evidence source_evidence_literature NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_assertion SIO_000772 15523652 NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_assertion wasDerivedFrom befree-2016 NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_assertion wasGeneratedBy ECO_0000203 NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.
- befree-2016 importedOn "2016-02-19" NP467283.RAMT9oi3ArMkoANzmhAUWor-2Csxum_kWTwVDDPIr_mBU130_provenance.