Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion> ?p ?o ?g. }
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- NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion type Assertion NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_head.
- NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion wasGeneratedBy ECO_0000203 NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_provenance.
- NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion wasDerivedFrom befree-2016 NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_provenance.
- NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion SIO_000772 9027848 NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_provenance.
- NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion evidence source_evidence_literature NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_provenance.
- NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_assertion description "[Merosin-deficient congenital muscular dystrophy (CMD) is caused by mutations in the laminin alpha 2 chain gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1367109.RAavtH6JvW0-Ex96KOUy8k3c6zHbmK3HVWj5PbpPIG0mQ130_provenance.