Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion> ?p ?o ?g. }
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- NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion type Assertion NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_head.
- NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion description "[Two genes have been identified for the X-linked forms (dystrophin and tafazzin), whereas three other genes (actin, lamin A/C, and desmin) cause autosomal dominant DCM; seven other loci for autosomal dominant DCM have been mapped but the genes have not been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_provenance.
- NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion evidence source_evidence_literature NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_provenance.
- NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion SIO_000772 10974018 NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_provenance.
- NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion wasDerivedFrom befree-20140225 NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_provenance.
- NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_assertion wasGeneratedBy ECO_0000203 NP640111.RADZSxIFPxxuJTbRnHVSiH8ltjLUXzy_8NfXq7eQQFfLU130_provenance.