Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_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." NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion evidence source_evidence_literature NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion SIO_000772 22833210 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion wasDerivedFrom befree-2016 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion wasGeneratedBy ECO_0000203 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.