Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_assertion> ?p ?o ?g. }
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- NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_assertion type Assertion NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_head.
- NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_assertion wasGeneratedBy ECO_0000218 NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_provenance.
- NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_assertion wasDerivedFrom uniprot-20150221 NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_provenance.
- NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_assertion SIO_000772 21376300 NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_provenance.
- NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_assertion evidence source_evidence_curated NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_provenance.
- NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_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." NP5206.RAfnoc68vjcH2trxVUvlkCPRGeNxEB5_F4PUH11zK8VOQ130_provenance.