Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion> ?p ?o ?g. }
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- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion type Assertion NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_head.
- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion wasGeneratedBy ECO_0000203 NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_provenance.
- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion wasDerivedFrom befree-20150227 NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_provenance.
- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion SIO_000772 18948003 NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_provenance.
- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion evidence source_evidence_literature NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_provenance.
- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_provenance.