Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_assertion description "[RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_assertion evidence source_evidence_literature NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_assertion SIO_000772 18571626 NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_assertion wasDerivedFrom gad-20150221 NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_assertion wasGeneratedBy ECO_0000203 NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP125077.RANmQeToTCKh_Pe7kGQ-uGYf_TdtB4ciSUxm1SATf6zpc130_provenance.