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- NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_assertion type Assertion NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_head.
- NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_assertion wasGeneratedBy ECO_0000203 NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_provenance.
- NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_assertion wasDerivedFrom befree-20140225 NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_provenance.
- NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_assertion SIO_000772 18310267 NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_provenance.
- NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_assertion evidence source_evidence_literature NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_provenance.
- NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_assertion description "[This case indicated the possibility of the occurrence of digenic inheritance in BS with SND resulting from double mutations in the CLCNKA and CLCNKB genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472098.RAjHeserMHbBupAMYfTrFUWh0KPkQH1IFxxB68Idzb2o0130_provenance.