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- source_evidence_literature type ECO_0000212 NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_assertion description "[Several reports show that DBA is associated with mutations in the ribosomal protein (RP) genes, RPS19, RPS24, RPS17, RPL35A, RPL5, RPL11, and RPS7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_assertion evidence source_evidence_literature NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_assertion SIO_000772 22510774 NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_assertion wasDerivedFrom befree-20140225 NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_assertion wasGeneratedBy ECO_0000203 NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP172620.RA24QkQHmd8XINBduh0Ou2z7p3_lhWAPJkvcqOSZl-pEE130_provenance.