Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_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." NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_assertion evidence source_evidence_curated NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_assertion SIO_000772 18469813 NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_assertion wasDerivedFrom ctd_human-2016 NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_assertion wasGeneratedBy ECO_0000218 NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP21717.RABp7pLMAtVRl7yyiM3koePFmcxKV5q_PIpvAdCUIRlps130_provenance.