Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion> ?p ?o ?g. }
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- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion type Assertion NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_head.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion description "[Two genes have been identified for the X-linked forms (dystrophin and tafazzin), while mutations in multiple genes cause autosomal dominant DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion evidence source_evidence_literature NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion SIO_000772 14567970 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion wasDerivedFrom befree-2016 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion wasGeneratedBy ECO_0000203 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.