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- source_evidence_literature type ECO_0000212 NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_assertion evidence source_evidence_literature NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_assertion SIO_000772 21810944 NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_assertion wasDerivedFrom befree-20150227 NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_assertion wasGeneratedBy ECO_0000203 NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626533.RAoXOL6eOV_D41hOPsw4UlObC4iTZ2adV6ofa6qG7QGk8130_provenance.