Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_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." NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_assertion evidence source_evidence_literature NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_assertion SIO_000772 15314642 NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_assertion wasDerivedFrom befree-2016 NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_assertion wasGeneratedBy ECO_0000203 NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP456267.RAc_vQgPDcDM8m-zp71L10dbM6R7xoZ_J0zgrmUrkSpoQ130_provenance.