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- source_evidence_literature type ECO_0000212 NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_assertion description "[Either GRIN2B or GRIN2A, encoding the NMDA receptor subunits NR2B and NR2A, was found to be disrupted by chromosome translocation breakpoints in individuals with mental retardation and/or epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_assertion evidence source_evidence_literature NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_assertion SIO_000772 20890276 NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_assertion wasDerivedFrom befree-20150227 NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_assertion wasGeneratedBy ECO_0000203 NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434506.RA9YPOhU7gYnNyud3VajwAONkzcd05fn24M0xiFE6nlLg130_provenance.