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- source_evidence_literature type ECO_0000212 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion description "[identified ACVRL1 mutations in hereditary hemorrhagic telangiectasia, including 4 unknown, and found that ACVRL1, and not ENG, mutations are predictive for liver disease]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion evidence source_evidence_literature NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion SIO_000772 18498373 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion wasDerivedFrom lhgdn-20090331 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion wasGeneratedBy ECO_0000203 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.