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- source_evidence_literature type ECO_0000212 NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_assertion description "[Interestingly, analyzing the regulatory network and mouse knockout expression data for NR4A2, a transcription factor previously associated with rare mutations in PD and here found as the most significantly under-expressed gene in PD among the jointly altered genes, suggests that aging-related NR4A2 expression changes may increase PD risk via downstream effects similar to disease-linked mutations and to expression changes in sporadic PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_assertion evidence source_evidence_literature NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_assertion SIO_000772 25447234 NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_assertion wasDerivedFrom befree-2016 NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_assertion wasGeneratedBy ECO_0000203 NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242169.RAA-af0xrmz3EF_yaDdLf9T8X0qj4NsYaYPeqEnsG618k130_provenance.