Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_assertion type Assertion NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_head.
- NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_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." NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_provenance.
- NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_assertion evidence source_evidence_literature NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_provenance.
- NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_assertion SIO_000772 25714449 NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_provenance.
- NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_assertion wasDerivedFrom befree-2016 NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_provenance.
- NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_assertion wasGeneratedBy ECO_0000203 NP1266257.RA6zLuWmPKf13aSpQ5-QHxBa7o584IJ-FVgUILNCrSdUc130_provenance.