Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion description "[Public databases also show that the EFHC1 P77T-R221H JME haplotype is present in unphenotyped West African ancestry populations, and we show that it can be found at appreciable frequency in healthy individuals with no family history of epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion evidence source_evidence_literature NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion SIO_000772 25489633 NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion wasDerivedFrom befree-2016 NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion wasGeneratedBy ECO_0000203 NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance.