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- source_evidence_literature type ECO_0000212 NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_assertion description "[This result suggests that 46,XY DSD patient phenotypes may be influenced by SRD5A2 polymorphism genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_assertion evidence source_evidence_literature NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_assertion SIO_000772 21631525 NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_assertion wasDerivedFrom befree-2016 NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_assertion wasGeneratedBy ECO_0000203 NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.
- befree-2016 importedOn "2016-02-19" NP898571.RAyrs0i5MkL_5xWr0eCJBjkdgB-LD2Y0e7sMN_mg7p0cw130_provenance.