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- NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_assertion type Assertion NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_head.
- NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_assertion wasGeneratedBy ECO_0000203 NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_provenance.
- NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_assertion wasDerivedFrom lhgdn-20090331 NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_provenance.
- NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_assertion SIO_000772 15563506 NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_provenance.
- NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_assertion evidence source_evidence_literature NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_provenance.
- NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_assertion description "[dominant mutations are common in Ullrich congenital muscular dystrophy (UCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207962.RA5shBSGkgYPwghRD6cD6mq5XM_ErIXMP2K0wOMX-Yj5g130_provenance.