Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_assertion description "[X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_assertion evidence source_evidence_curated NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_assertion SIO_000772 18469813 NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_assertion wasDerivedFrom ctd_human-2016 NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_assertion wasGeneratedBy ECO_0000218 NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP21716.RAlxSg32mKCPpKL18LqrVMISQF3iOxQgD8eIR3WeJ-7pM130_provenance.