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- NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_assertion type Assertion NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_head.
- NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_assertion wasGeneratedBy ECO_0000203 NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_provenance.
- NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_assertion wasDerivedFrom befree-2016 NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_provenance.
- NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_assertion SIO_000772 9270600 NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_provenance.
- NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_assertion evidence source_evidence_literature NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_provenance.
- NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_assertion description "[Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1379397.RA0HF-eMravASgtXfl21vilA0GwBY413IHjPRQ_t7jKKk130_provenance.