Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_assertion> ?p ?o ?g. }
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- NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_assertion type Assertion NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_head.
- NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_assertion wasGeneratedBy ECO_0000203 NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_provenance.
- NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_assertion wasDerivedFrom gad-20150221 NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_provenance.
- NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_assertion SIO_000772 16199542 NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_provenance.
- NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_assertion evidence source_evidence_literature NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_provenance.
- NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_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." NP96171.RAzuwsfdLd7VTqCZpW57ANaPFxJ2kmHiDJNQM9pvpL_Ek130_provenance.