Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion> ?p ?o ?g. }
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- NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion type Assertion NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_head.
- NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion description "[PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_provenance.
- NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion evidence source_evidence_literature NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_provenance.
- NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion SIO_000772 22243967 NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_provenance.
- NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion wasDerivedFrom befree-2016 NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_provenance.
- NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_assertion wasGeneratedBy ECO_0000203 NP953109.RA2bzpP7vtbs6P8H8G3_eTm03bxsiL73fWtqxbkkvybO4130_provenance.