Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion> ?p ?o ?g. }
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- NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion type Assertion NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_head.
- NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion wasGeneratedBy ECO_0000203 NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_provenance.
- NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion wasDerivedFrom befree-2016 NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_provenance.
- NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion SIO_000772 22468107 NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_provenance.
- NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion evidence source_evidence_literature NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_provenance.
- NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_assertion description "[The patients with dysferlinopathy were classified by initial muscle weakness: fifteen patients with Miyoshi myopathy phenotype (MM), thirteen patients with limb girdle muscular dystrophy 2B phenotype (LGMD2B), two patients with proximodistal phenotype, and one asymptomatic patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971883.RAkOAJdyfXrEcxzclVx_viTDKMYrIm1a-R_xKzIGFvx3k130_provenance.