Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_assertion description "[Recessive GJA1 mutations cause Hallermann-Streiff syndrome, a disorder showing substantial overlap with ODDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_assertion evidence source_evidence_literature NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_assertion SIO_000772 21871435 NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_assertion wasDerivedFrom befree-2016 NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_assertion wasGeneratedBy ECO_0000203 NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.
- befree-2016 importedOn "2016-02-19" NP919547.RADAD41p--Ze5wQE5doj0KUf9I3lNJB5Y-Zigm6wDkiqM130_provenance.