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- NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_assertion type Assertion NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_head.
- NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_assertion wasGeneratedBy ECO_0000203 NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_provenance.
- NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_assertion wasDerivedFrom befree-20140225 NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_provenance.
- NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_assertion SIO_000772 12107438 NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_provenance.
- NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_assertion evidence source_evidence_literature NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_provenance.
- NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_assertion description "[We conclude that mutations of USHIC can cause both Usher syndrome type IC and nonsyndromic recessive deafness DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495903.RADssbc8KV1TTgXJxQDxsSB0ibtSBAZ9ULCv1emnUDpUQ130_provenance.