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- source_evidence_literature type ECO_0000212 NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_assertion description "[We have explored the application of array-CGH to the detection of such changes on a set of 20 samples consisting of patients with eye diseases associated with changes on chromosome 6p25 together with unaffected individuals, as well as two samples from tuberous sclerosis 2 (TSC2)-affected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_assertion evidence source_evidence_literature NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_assertion SIO_000772 15221791 NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_assertion wasDerivedFrom befree-2016 NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_assertion wasGeneratedBy ECO_0000203 NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP450003.RAgMity31vTYmRxqGern0-ty1tU1Ml9OR1v4VM6ZuEP-Q130_provenance.