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- source_evidence_literature type ECO_0000212 NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_assertion wasGeneratedBy ECO_0000203 NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_assertion wasDerivedFrom befree-20140225 NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_assertion SIO_000772 15314642 NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_assertion evidence source_evidence_literature NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_assertion description "[Using a bioinformatic screen for ciliary genes in combination with mutational analyses, we identified ARL6 as the gene underlying Bardet-Biedl syndrome type 3, a multisystemic disorder characterized by obesity, blindness, polydactyly, renal abnormalities and cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP197179.RAJXarLwaBP3Nax35wJrmepei_M5SpfvLuBICUwQRBaS4130_provenance.