Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion> ?p ?o ?g. }
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- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion type Assertion NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_head.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion wasGeneratedBy ECO_0000218 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion wasDerivedFrom uniprot-20130724 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion SIO_000772 18625862 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion evidence source_evidence_curated NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- 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.