Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_assertion description "[Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_assertion evidence source_evidence_curated NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_assertion SIO_000772 10802654 NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_assertion wasDerivedFrom ctd_human-20150221 NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_assertion wasGeneratedBy ECO_0000218 NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP31918.RAtUYeZWkimLroUi_-g6rN1CjWxa3YWprmtmcogLRUluY130_provenance.