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- source_evidence_literature type ECO_0000212 NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_assertion description "[Mutations in the CDKL5 gene (also known as STK9) have recently been shown to cause early onset epilepsy and severe mental retardation (ISSX or West syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_assertion evidence source_evidence_literature NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_assertion SIO_000772 16015284 NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_assertion wasDerivedFrom befree-2016 NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_assertion wasGeneratedBy ECO_0000203 NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.
- befree-2016 importedOn "2016-02-19" NP503957.RAsU2LgLSKA7J9Bv2Dkbzuvs2HcmrcmSRFKmk7UnyzNxA130_provenance.