Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_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." NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_assertion evidence source_evidence_literature NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_assertion SIO_000772 11955795 NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_assertion wasDerivedFrom befree-2016 NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_assertion wasGeneratedBy ECO_0000203 NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.
- befree-2016 importedOn "2016-02-19" NP351920.RAHHtgTxh98E0PP0scsjkSC363WWfUjPAI5M7vcgJ3fyg130_provenance.