Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion> ?p ?o ?g. }
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- NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion type Assertion NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_head.
- NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion description "[These include lamin A/C in autosomal dominant Emery-Dreifuss muscular dystrophy, SMN in spinal muscular atrophy, SIX5 in myotonic dystrophy, calpain3 in type 2A limb-girdle muscular dystrophy, PABP2 in oculopharyngeal dystrophy, androgen receptor in spinal and bulbar muscular atrophy and the ataxins in hereditary ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_provenance.
- NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion evidence source_evidence_literature NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_provenance.
- NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion SIO_000772 10838245 NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_provenance.
- NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion wasDerivedFrom befree-20150227 NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_provenance.
- NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_assertion wasGeneratedBy ECO_0000203 NP974907.RA-8VVAVz-o14sI9R6wzZhwskDH7QRu_tQ439cpS9ZGvU130_provenance.