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- source_evidence_literature type ECO_0000212 NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_assertion description "[The cblD gene was localized to human chromosome 2q23.2, and a candidate gene, designated MMADHC (methylmalonic aciduria, cblD type, and homocystinuria), was identified in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_assertion evidence source_evidence_literature NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_assertion SIO_000772 18385497 NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_assertion wasDerivedFrom befree-20150227 NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_assertion wasGeneratedBy ECO_0000203 NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887375.RABz1WyMqaybRDLK_JOAe7qCwjWiw38nYBxtqdkN1FwJ4130_provenance.