Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion> ?p ?o ?g. }
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- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion type Assertion NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_head.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_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." NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion evidence source_evidence_literature NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion SIO_000772 14567970 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion wasDerivedFrom befree-20140225 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion wasGeneratedBy ECO_0000203 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.