Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1223143.RA1A0A2TBaTdXPG42JpGEKXWPfNB3p_5XB8NiGFKWiXmU130_provenance.