Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion> ?p ?o ?g. }
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- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion type Assertion NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_head.
- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_provenance.
- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion evidence source_evidence_literature NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_provenance.
- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion SIO_000772 15947064 NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_provenance.
- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion wasDerivedFrom befree-20140225 NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_provenance.
- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion wasGeneratedBy ECO_0000203 NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_provenance.