Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_assertion description "[Six1 is a crucial regulator of renal development: mutations in human SIX1 cause branchio-oto-renal (BOR) syndrome and Six1(-/-) mice exhibit renal agenesis, although the ureter is present.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_assertion evidence source_evidence_literature NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_assertion SIO_000772 20110314 NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_assertion wasDerivedFrom befree-2016 NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_assertion wasGeneratedBy ECO_0000203 NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.
- befree-2016 importedOn "2016-02-19" NP790132.RAAUao1VgDpjhrdg6aGyhKOffWfK3PEg8gr5OtAL4Ew-o130_provenance.