Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion> ?p ?o ?g. }
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- NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion type Assertion NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_head.
- NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion description "[A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_provenance.
- NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion evidence source_evidence_literature NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_provenance.
- NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion SIO_000772 25524373 NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_provenance.
- NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion wasDerivedFrom befree-2016 NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_provenance.
- NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_assertion wasGeneratedBy ECO_0000203 NP1249443.RAGRLfaC0wXrgAUyXYCuVlA_H0m0NPC6hhEU85Q8nkwQE130_provenance.