Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion> ?p ?o ?g. }
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- NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion type Assertion NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_head.
- NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion wasGeneratedBy ECO_0000203 NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_provenance.
- NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion wasDerivedFrom befree-20140225 NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_provenance.
- NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion SIO_000772 16421216 NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_provenance.
- NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion evidence source_evidence_literature NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_provenance.
- NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_assertion description "[Congenital chloride diarrhoea (CLD) is a rare inherited disease caused by mutations in the solute carrier family 26 member 3 (SLC26A3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801832.RA3tVYDxXe6i_chLDTkWtr17xiXFMZ2IgQ2jsrgzBoX88130_provenance.