Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_assertion description "[Unexpectedly, we found that deleting exons 2-4 of Dyx1c1 in mice caused a phenotype resembling primary ciliary dyskinesia (PCD), a disorder characterized by chronic airway disease, laterality defects and male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_assertion evidence source_evidence_curated NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_assertion SIO_000772 23872636 NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_assertion wasDerivedFrom ctd_human-20150221 NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_assertion wasGeneratedBy ECO_0000218 NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP13097.RAPL0aFCZl0vjqjvw4ks-pQHYcvGyFe8df2J95caM4iZE130_provenance.