Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_assertion> ?p ?o ?g. }
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- NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_assertion type Assertion NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_head.
- NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_assertion wasGeneratedBy ECO_0000203 NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_provenance.
- NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_assertion wasDerivedFrom befree-20140225 NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_provenance.
- NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_assertion SIO_000772 9270600 NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_provenance.
- NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_assertion evidence source_evidence_literature NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_provenance.
- NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_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." NP611491.RAeBRVQHVj2XDd9j2a8MbiHFYy0I1502C2knR_lz55ZaI130_provenance.