Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion> ?p ?o ?g. }
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- NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion type Assertion NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_head.
- NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion description "[GRIN2A mutations cause epilepsy-aphasia spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion evidence source_evidence_curated NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion SIO_000772 23933818 NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion wasDerivedFrom uniprot-20150221 NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_assertion wasGeneratedBy ECO_0000218 NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.