Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion> ?p ?o ?g. }
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- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion type Assertion NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_head.
- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_provenance.
- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion evidence source_evidence_literature NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_provenance.
- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion SIO_000772 18479388 NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_provenance.
- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion wasDerivedFrom lhgdn-20090331 NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_provenance.
- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion wasGeneratedBy ECO_0000203 NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_provenance.