Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion> ?p ?o ?g. }
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- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion type Assertion NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_head.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion description "[Limb-girdle muscular dystrophy 1A (LGMD1A [MIM 159000]) is an autosomal dominant form of muscular dystrophy characterized by adult onset of proximal weakness progressing to distal muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion evidence source_evidence_literature NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion SIO_000772 12428213 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion wasDerivedFrom befree-20150227 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion wasGeneratedBy ECO_0000203 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.