Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_assertion wasGeneratedBy ECO_0000203 NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_assertion wasDerivedFrom befree-20140225 NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_assertion SIO_000772 12436196 NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_assertion evidence source_evidence_literature NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_assertion description "[We studied 19 patients of Southeast Asian (SEA) ethnic ancestry with Leber's hereditary optic neuropathy (LHON) to investigate the mtDNA haplotypes associated with the primary mutation(s).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625495.RAi4f_h8kqF3nWkEX41VjPZcJwovNO78BOLHAyKIIUC5w130_provenance.