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- source_evidence_literature type ECO_0000212 NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_assertion evidence source_evidence_literature NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_assertion SIO_000772 10691109 NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_assertion wasDerivedFrom befree-20150227 NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_assertion wasGeneratedBy ECO_0000203 NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.