Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_assertion description "[BOR syndrome is an autosomal dominant trait encompassing branchial, otic and renal anomalies because of mutations in EYA1, SIX1 and SIX5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_assertion evidence source_evidence_literature NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_assertion SIO_000772 18177466 NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_assertion wasDerivedFrom befree-20140225 NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_assertion wasGeneratedBy ECO_0000203 NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP752514.RAr_njB1PMKg_RuuePN4ptzsw711lK_iur6m6mNZTImiA130_provenance.