Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion> ?p ?o ?g. }
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- NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion type Assertion NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_head.
- NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion description "[Together, these findings indicate that mutations in the gene encoding LMOD3 underlie congenital myopathy and demonstrate that LMOD3 is essential for the organization of sarcomeric thin filaments in skeletal muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion evidence source_evidence_literature NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion SIO_000772 25250574 NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion wasDerivedFrom befree-2016 NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_assertion wasGeneratedBy ECO_0000203 NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.