Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_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." NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_assertion evidence source_evidence_curated NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_assertion SIO_000772 18469813 NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_assertion wasDerivedFrom ctd_human-20150221 NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_assertion wasGeneratedBy ECO_0000218 NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP25298.RAdMUjFtWEyYbk0mWX5X5y3VkfcvUwQdIJGlR0i0BvNIo130_provenance.