Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion description "[Mutations in myotilin gene (MYOT) have been associated with variable syndromes including limb girdle muscular dystrophy type 1A (LGMD1A) and a subgroup of myofibrillar myopathy (MFM/MYOT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion evidence source_evidence_literature NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion SIO_000772 15947064 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion wasDerivedFrom befree-20140225 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion wasGeneratedBy ECO_0000203 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.