Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_assertion description "[In this retrospective cross-sectional study clinical and muscle imaging data of patients with Miyoshi distal myopathy phenotype (MMD1 and MMD3) and limb girdle muscular dystrophy 2L (LGMD2L) were described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_assertion evidence source_evidence_literature NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_assertion SIO_000772 25176504 NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_assertion wasDerivedFrom befree-2016 NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_assertion wasGeneratedBy ECO_0000203 NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215840.RArLl59vUEga5wPIcmYV7sV4m4Lm1nSI7de1zRRRIKHOo130_provenance.