Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_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." NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_assertion evidence source_evidence_curated NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_assertion SIO_000772 20890276 NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_assertion wasDerivedFrom ctd_human-2016 NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_assertion wasGeneratedBy ECO_0000218 NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP27294.RAb1M8ktW_qPIQSJOq0XhyUpzcMw3Ui6t_JQoCUitfqoc130_provenance.