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- source_evidence_literature type ECO_0000212 NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_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." NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_assertion evidence source_evidence_literature NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_assertion SIO_000772 15221791 NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_assertion wasDerivedFrom befree-20140225 NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_assertion wasGeneratedBy ECO_0000203 NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP759419.RAiF334C5gsaC5Ysmu3Cn5UwCKzW7BxJkOR9L_FN1K3s8130_provenance.