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- source_evidence_literature type ECO_0000212 NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_assertion description "[Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_assertion evidence source_evidence_literature NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_assertion SIO_000772 17767372 NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_assertion wasDerivedFrom befree-20150227 NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_assertion wasGeneratedBy ECO_0000203 NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP991905.RA9tIbGw_WXh31_aSdBpRr_G245yPVri5DKOe5VellwoM130_provenance.