Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_assertion wasGeneratedBy ECO_0000218 NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_assertion wasDerivedFrom uniprot-2016 NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_assertion SIO_000772 21376300 NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_assertion evidence source_evidence_curated NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.
- NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_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." NP6558.RAB3sHzjAl955X3sFryBLnv-8E50t_427565ZbvwTtcSY130_provenance.