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- source_evidence_literature type ECO_0000212 NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_assertion description "[We studied the association of a promoter variant (-86C/T) and three intronic polymorphisms, rs883473, rs6494223 and rs904952, in the non-duplicated region of CHRNA7 with sustained attention in 143 euthymic BD patients (based on DSM-IV criteria) and 101 healthy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_assertion evidence source_evidence_literature NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_assertion SIO_000772 21550667 NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_assertion wasDerivedFrom befree-20140225 NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_assertion wasGeneratedBy ECO_0000203 NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615786.RAZfEbf4KfctZcuXbOhP-eXm0nDsmgVMIxf0qFZzKPPIA130_provenance.