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- source_evidence_literature type ECO_0000212 NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_assertion description "[It also extends the phenotypical heterogeneity associated with LHX4 mutations, which includes variable anterior pituitary hormone deficits, as well as pituitary and extrapituitary abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_assertion evidence source_evidence_literature NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_assertion SIO_000772 18445675 NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_assertion wasDerivedFrom befree-2016 NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_assertion wasGeneratedBy ECO_0000203 NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.
- befree-2016 importedOn "2016-02-19" NP668513.RAM89auokmxAo-jj2VJkCduO2FpgQXngvFjjiUIwU64f8130_provenance.