Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_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." NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_assertion evidence source_evidence_curated NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_assertion SIO_000772 18469813 NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_assertion wasDerivedFrom ctd_human-20130708 NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_assertion wasGeneratedBy ECO_0000218 NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP25485.RAeN6RFqRkBySb6Lh67OCvVzZ8acPeerRORUY6dGwo-M8130_provenance.