Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_assertion description "[Increased numbers of coassembled PSD-95 to NMDA-receptor subunits NR2B and NR1 in human epileptic cortical dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_assertion evidence source_evidence_literature NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_assertion SIO_000772 15030493 NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_assertion wasDerivedFrom befree-2016 NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_assertion wasGeneratedBy ECO_0000203 NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP436298.RAgM-QYssz5Tsj-TLr1O5WbGYGGn_w-SQv-u_EanDpCmQ130_provenance.