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- source_evidence_literature type ECO_0000212 NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_assertion wasGeneratedBy ECO_0000203 NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_assertion wasDerivedFrom befree-2016 NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_assertion SIO_000772 17319270 NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_assertion evidence source_evidence_literature NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.
- NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_assertion description "[CBS gene G919A mutation is associated with the development of CHD, and the mutated allele may decrease the risk of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595599.RA3_NfS6Ouc96719Ck0840t6HlinmbKPiv9dYEOJPHWqQ130_provenance.