Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion evidence source_evidence_literature NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion SIO_000772 22833210 NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion wasDerivedFrom befree-20140225 NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion wasGeneratedBy ECO_0000203 NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.