Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion type Assertion NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_head.
- NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion wasGeneratedBy ECO_0000203 NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_provenance.
- NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion wasDerivedFrom gad-20130706 NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_provenance.
- NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion SIO_000772 16199542 NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_provenance.
- NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion evidence source_evidence_literature NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_provenance.
- NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_assertion description "[ Multiple gene mutations occurring in HCM families may result in a more severe clinical phenotype because of a double dose effect. This highlights the importance of screening the entire panel of HCM genes even after a single mutation has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58583.RAl12Ampc9TiUvAb5S3-DmXTSVVCLOoBffhtRafxdE178130_provenance.