Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion type Assertion NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_head.
- NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion description "[Inactivating mutations in either of the related EVER1/TMC6 and EVER2/TMC8 genes cause most EV cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_provenance.
- NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion evidence source_evidence_literature NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_provenance.
- NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion SIO_000772 18727487 NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_provenance.
- NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion wasDerivedFrom befree-20140225 NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_provenance.
- NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_assertion wasGeneratedBy ECO_0000203 NP717672.RAd6LCywxBQ7s4UGSYFAazQLFFagmHEsYlMxzAXr1cr58130_provenance.