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- source_evidence_literature type ECO_0000212 NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_assertion wasGeneratedBy ECO_0000203 NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_assertion wasDerivedFrom lhgdn-20090331 NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_assertion SIO_000772 16542389 NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_assertion evidence source_evidence_literature NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
- NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.