Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_assertion description "[Independently, we also identified compound heterozygous WDR19 mutations by exome sequencing in a Moroccan family with isolated nephronophthisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_assertion evidence source_evidence_literature NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_assertion SIO_000772 22019273 NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_assertion wasDerivedFrom befree-20140225 NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_assertion wasGeneratedBy ECO_0000203 NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP670274.RAXHK91PdFL6HL0J5_WhOjlzsb28Zbq--s56sn_r9bXnA130_provenance.