Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion> ?p ?o ?g. }
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- NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion type Assertion NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_head.
- NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion description "[The spectacular progress concerning dystrophin and its pathology, the dystrophinopathies, has led to a somewhat arbitrarily separated heterogeneous group of nondystrophinopathic muscular dystrophies that currently comprise the Emery-Dreifuss type, the nosologically heterogeneous autosomal-recessive limb-girdle muscular dystrophy, the severe childhood autosomal-recessive muscular dystrophy, the merosin-positive and -negative congenital muscular dystrophies, the autosomal-recessive distal muscular dystrophy of Miyoshi, the facio-scapulo-humeral muscular dystrophy, and myotonic dystrophy, both the adult and neonatal variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_provenance.
- NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion evidence source_evidence_literature NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_provenance.
- NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion SIO_000772 8795845 NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_provenance.
- NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion wasDerivedFrom befree-2016 NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_provenance.
- NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_assertion wasGeneratedBy ECO_0000203 NP1357052.RA8NWEu3fvJGeZ0cw1DuenrHscmfIzT_d4hDhpB74ajgg130_provenance.