Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion description "[These findings suggest that (i) three tic factors can be discerned with a distinct underlying genetic architecture and that (ii) considering the low tic heritabilities found, only focusing on the narrow-sense TS phenotype and leaving out comorbidities that are part of the broader sense tic phenotype may lead to missing heritability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion evidence source_evidence_literature NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion SIO_000772 25714449 NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion wasDerivedFrom befree-2016 NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion wasGeneratedBy ECO_0000203 NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_provenance.