Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_assertion> ?p ?o ?g. }
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- NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_assertion type Assertion NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_head.
- NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_assertion wasGeneratedBy ECO_0000218 NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_provenance.
- NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_assertion wasDerivedFrom uniprot-20130724 NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_provenance.
- NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_assertion SIO_000772 21376300 NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_provenance.
- NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_assertion evidence source_evidence_curated NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_provenance.
- NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_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." NP884.RAE4XAAfMWevOD977K600zbQL82Z2wM7buU7HzbSeDBlE130_provenance.