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- source_evidence_literature type ECO_0000212 NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_assertion description "[Four patients had an identified genetic mutation (McCune-Albright syndrome: n = 1; MEN1: n = 1; AIP: n = 2); the remaining three cases were sporadic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_assertion evidence source_evidence_literature NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_assertion SIO_000772 22024364 NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_assertion wasDerivedFrom befree-20150227 NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_assertion wasGeneratedBy ECO_0000203 NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP553492.RA5sys5HnLjZWQBV9alrinFUr-1oH6aXk5pLNyuBIgSYU130_provenance.