Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion> ?p ?o ?g. }
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- NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion type Assertion NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_head.
- NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion description "[GRIN2A mutations cause epilepsy-aphasia spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_provenance.
- NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion evidence source_evidence_curated NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_provenance.
- NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion SIO_000772 23933818 NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_provenance.
- NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion wasDerivedFrom uniprot-2016 NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_provenance.
- NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_assertion wasGeneratedBy ECO_0000218 NP7619.RAKMETsViSnYFQAEowFvTT9xfxOP4uEN9qkQvp1-QUEfA130_provenance.