Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion type Assertion NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_head.
- NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion description "[Central core disease (CCD), congenital fibre type disproportion (CFTD), and nemaline myopathy (NM) are earlyonset clinically heterogeneous congenital myopathies, characterized by generalized muscle weakness and hypotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_provenance.
- NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion evidence source_evidence_literature NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_provenance.
- NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion SIO_000772 19206168 NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_provenance.
- NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion wasDerivedFrom befree-20140225 NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_provenance.
- NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_assertion wasGeneratedBy ECO_0000203 NP556600.RABgnS2Hx7GXTzzHtR7hCGSfiSgG5OtV7GhhFxi3q-1TI130_provenance.