Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_assertion description "[Although initially thought to be within the same spectrum as severe myoclonic epilepsy of infancy, the exclusion of SCN1A mutations in non-generalized epilepsy with febrile seizures plus (GEFS+) MAE cases has confirmed the genetic distinction of MAE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_assertion evidence source_evidence_literature NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_assertion SIO_000772 22780699 NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_assertion wasDerivedFrom befree-20150227 NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_assertion wasGeneratedBy ECO_0000203 NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682509.RA7aGiCIXp8smt3s45SJ5GHoNT8r3wP9635SGx2CXiWuk130_provenance.