Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_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." NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_assertion evidence source_evidence_curated NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_assertion SIO_000772 18469813 NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_assertion wasDerivedFrom uniprot-20130724 NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_assertion wasGeneratedBy ECO_0000218 NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4817.RAWuWNuOfCA7pbO9Y64YJt0-nYwmAZ-sSTgWb_VNHD074130_provenance.