Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.
- 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.
- uniprot-20150221 importedOn "2015-02-21" NP3405.RAHbqhAjdJ2F0O51Oc59S2cvpzPjoizfWikWgBaYADaRM130_provenance.