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- source_evidence_literature type ECO_0000212 NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- befree-2016 importedOn "2016-02-19" NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_assertion wasGeneratedBy ECO_0000203 NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_assertion wasDerivedFrom befree-2016 NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_assertion SIO_000772 19508727 NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_assertion evidence source_evidence_literature NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_assertion description "[The genotype-phenotype correlation was consistent with a higher 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." NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.