Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric diso]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_assertion evidence source_evidence_literature NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_assertion SIO_000772 20398908 NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_assertion wasDerivedFrom gad-20150221 NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_assertion wasGeneratedBy ECO_0000203 NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP173022.RAQTmlRLiE9oQPpYWjeBammoDKRmQ8aJ5Y5UX23AWdDfU130_provenance.