Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_assertion description "[Recent genetic studies have investigated associations between ICD and polymorphisms of genes involved in the dopamine metabolism pathway (COMT, DAT), dopamine receptors (DRD1, DRD2, DRD3, DRD4), serotonin receptors and its transporter (HTR2A, 5HTT), and glutamate receptors (GRIN2B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_assertion evidence source_evidence_literature NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_assertion SIO_000772 23232665 NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_assertion wasDerivedFrom befree-20140225 NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_assertion wasGeneratedBy ECO_0000203 NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP684524.RAD_UDLm56ZFQFx0TAcgX41bZ4bR3CTowKUbylP_-xCaM130_provenance.