Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion> ?p ?o ?g. }
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- NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_assertion type Assertion NP1266258.RANJjP8KvGIUcByzq0Lg8WRJfcCUWRV3ah-XKii84yVnA130_head.
- 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.