Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_assertion description "[Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_assertion evidence source_evidence_literature NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_assertion SIO_000772 22019273 NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_assertion wasDerivedFrom befree-2016 NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_assertion wasGeneratedBy ECO_0000203 NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.
- befree-2016 importedOn "2016-02-19" NP932807.RAUkFr38RqQZOn5OYN40N-ozrR17jYqq7UrDEkLA9CkR4130_provenance.