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- NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_assertion type Assertion NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_head.
- NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_assertion wasGeneratedBy ECO_0000203 NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_provenance.
- NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_assertion wasDerivedFrom befree-20140225 NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_provenance.
- NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_assertion SIO_000772 12107438 NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_provenance.
- NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_assertion evidence source_evidence_literature NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_provenance.
- NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_assertion description "[Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922233.RAlFCSZ-10_RGvWWzEBUeszKQ8Sp82auLzdwNj6tBRN70130_provenance.