Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_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." NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_assertion evidence source_evidence_literature NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_assertion SIO_000772 20890276 NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_assertion wasDerivedFrom befree-20140225 NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_assertion wasGeneratedBy ECO_0000203 NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP480331.RA6nxqh05J6HaCXfkn0CpcAM8ruUlsfj96QfNEULSFANE130_provenance.