Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_assertion description "[The results demonstrate that KIF21A mutations are a rare cause of CFEOM3 (congenital fibrosis of the extraocular muscles) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_assertion evidence source_evidence_literature NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_assertion SIO_000772 15223798 NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_assertion wasDerivedFrom lhgdn-20090331 NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_assertion wasGeneratedBy ECO_0000203 NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.