Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP895105.RAflzzig1oqc8i5vbm3bKKb-qf4QO-tVVhp-niPpZCX-o130_provenance.