Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_assertion description "[Mutations in the genes encoding each of the other components of the skeletal muscle sarcospan-sarcoglycan complex (alpha - delta sarcoglycan) have been shown to cause limb girdle muscular dystrophy (LGMD2C-F).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_assertion evidence source_evidence_literature NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_assertion SIO_000772 11180757 NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_assertion wasDerivedFrom befree-2016 NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_assertion wasGeneratedBy ECO_0000203 NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.
- befree-2016 importedOn "2016-02-19" NP307491.RAHaQridHff6Fb5e4oolUC3Nytpi-jSOpERLlxVGX6e_o130_provenance.