Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_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." NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_assertion evidence source_evidence_literature NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_assertion SIO_000772 11955795 NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_assertion wasDerivedFrom befree-2016 NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_assertion wasGeneratedBy ECO_0000203 NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.
- befree-2016 importedOn "2016-02-19" NP351924.RAcWOrMzIwO6q4j_fp46g6AlajE6FuldQ5F4Kg0roHakg130_provenance.