Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_assertion wasGeneratedBy ECO_0000218 NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_assertion wasDerivedFrom uniprot-20150221 NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_assertion SIO_000772 21376300 NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_assertion evidence source_evidence_curated NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.
- NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_assertion description "[Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4698.RANESbrhWcrPY6P8TV1dLesXynZga1HXHqV2DJ7xCRc4A130_provenance.