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- source_evidence_literature type ECO_0000212 NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_assertion description "[This population was enriched in genes involved in cell migration, axonal guidance, neurogenesis, and regulation of transcription and includes genes implicated in autism, epilepsy, and mental retardation; all features recognized in patients with ARX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_assertion evidence source_evidence_literature NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_assertion SIO_000772 18799476 NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_assertion wasDerivedFrom befree-20150227 NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_assertion wasGeneratedBy ECO_0000203 NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978102.RAGyLZFTOGg18w_cyQztU8On-T8PlVrPWox1b1ZK6cbW8130_provenance.