Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_assertion description "[The present study explores whether the PRRT2 mutation is a potential cause of febrile seizures, including febrile seizures plus (FS+), generalized epilepsy with febrile seizures plus (GEFS+) and Dravet syndrome (DS); thus, it may provide a new drug target for personalized medicine for febrile seizure patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_assertion evidence source_evidence_literature NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_assertion SIO_000772 25522171 NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_assertion wasDerivedFrom befree-2016 NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_assertion wasGeneratedBy ECO_0000203 NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249241.RA370X2bsq7TqAIJg21NuJ5rThL_RpNNrkm1cqMzWQNBU130_provenance.