Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_assertion description "[As the CRYGA mutation did not explain the cataract, several other candidate loci (CCV, GJA8, CRYBB2, BFSP2, MIP, GJA8, CENTRAL POUCH-LIKE, CRYBA1) were investigated by microsatellite markers and linkage analysis, but they were excluded based on the combination of haplotype analysis and two-point linkage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_assertion evidence source_evidence_literature NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_assertion SIO_000772 12646746 NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_assertion wasDerivedFrom befree-20140225 NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_assertion wasGeneratedBy ECO_0000203 NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381623.RAyfLLKWVIAThiPxgJnK3uK12wNkch2uLz1YqiPFzgUOk130_provenance.