Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_assertion description "[Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_assertion evidence source_evidence_curated NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_assertion SIO_000772 20890276 NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_assertion wasDerivedFrom uniprot-20150221 NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_assertion wasGeneratedBy ECO_0000218 NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3443.RAz3MwnggZrLAl56edvtLQWJtcO6cGQo57R9QcAZ8G4Io130_provenance.