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- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion type Assertion NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_head.
- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion wasGeneratedBy ECO_0000203 NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_provenance.
- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion wasDerivedFrom befree-20140225 NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_provenance.
- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion SIO_000772 22427994 NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_provenance.
- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion evidence source_evidence_literature NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_provenance.
- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion description "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_provenance.