Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_assertion description "[Thus, we have corroborated a prediction from the model of ABCR pathogenicity that (1) one mutant ABCR allele is always missense in late-onset STGD1 patients, and (2) the age-of-onset is correlated with the amount of ABCR activity of this allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_assertion evidence source_evidence_literature NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_assertion SIO_000772 11379881 NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_assertion wasDerivedFrom befree-20140225 NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_assertion wasGeneratedBy ECO_0000203 NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP299902.RAkQ-fslwmffNtXuqFdEdtD1B9Plk5KX2fygst5ma16Lw130_provenance.