Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion> ?p ?o ?g. }
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- NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_assertion type Assertion NP789600.RAX055CceSmaWzVM0q08X5aNtMSj3swH30xmGerwTLmUA130_head.
- 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.