Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_assertion description "[Various mutations within the epsilon-sarcoglycan (SGCE) gene have been associated with M-D, but mutations are detected in only about 30% of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_assertion evidence source_evidence_literature NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_assertion SIO_000772 19066193 NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_assertion wasDerivedFrom befree-20140225 NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_assertion wasGeneratedBy ECO_0000203 NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP243037.RAJTI47oIRr8xvRupHwrsQZM8rpbVUt2SAteJ6T_ce_3k130_provenance.