Matches in Nanopublications for { ?s ?p "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP817595.RAdEsXY8xSyxKZX9ocMIUrF3GPLfKU_Ws3pogSoVcyU6M130_assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817595.RAdEsXY8xSyxKZX9ocMIUrF3GPLfKU_Ws3pogSoVcyU6M130_provenance.
- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_provenance.
- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_provenance.