Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_assertion> ?p ?o ?g. }
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- NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_assertion type Assertion NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_head.
- NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_assertion wasGeneratedBy ECO_0000203 NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_assertion wasDerivedFrom befree-20140225 NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_assertion SIO_000772 16421216 NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_assertion evidence source_evidence_literature NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_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." NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.