Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_assertion wasGeneratedBy ECO_0000203 NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_assertion wasDerivedFrom lhgdn-20090331 NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_assertion SIO_000772 17579882 NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_assertion evidence source_evidence_literature NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_assertion description "[A novel mutation of the OPA1 gene was detected in a Japanese patient with autosomal dominant optic atrophy (ADOA) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP146669.RARsI56Wc_iXDKulw34im13hSnYfObiHVeeyU9mZJULQ0130_provenance.