Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_assertion description "[Carriage of a mutant catechol-O-methyltransferase (COMT) allele is associated with breast cancer, neurologic disorders such as Parkinson's disease, and modulates behavior among patients with schizophrenia, alcoholics and the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_assertion evidence source_evidence_literature NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_assertion SIO_000772 11955795 NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_assertion wasDerivedFrom befree-20150227 NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_assertion wasGeneratedBy ECO_0000203 NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP321662.RAO1O1rNtJ_FLC07p3cvY6K8rS3oEoMDZJCAvAcpJ3ZFU130_provenance.