Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion description "[The search for potential candidate genes within the 8-Mb overlapping homozygous region in these families revealed the presence of CLRN1, a gene previously known to cause Usher's syndrome type III (USH3), which was analyzed by direct sequence analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion evidence source_evidence_literature NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion SIO_000772 21310491 NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion wasDerivedFrom befree-20140225 NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion wasGeneratedBy ECO_0000203 NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_provenance.