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- source_evidence_literature type ECO_0000212 NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_assertion description "[mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_assertion evidence source_evidence_literature NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_assertion SIO_000772 17967976 NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_assertion wasDerivedFrom lhgdn-20090331 NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_assertion wasGeneratedBy ECO_0000203 NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212280.RA5rM4heZ61IKNxbv-et38fyAJCiSCRzG7mm-M_Y_YaWw130_provenance.