Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_assertion description "[Neuron-specific mapping of the genome-wide distribution of H3K4me3 revealed 136 differentially enriched loci associated with genes implicated in neuronal development and neurodegeneration, including GPR3, TMEM106B, PDIA6 and the Notch signaling genes hairy and enhancer of split 4 (HES4) and JAGGED2, supporting the view that the neuronal epigenome is affected in HD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_assertion evidence source_evidence_literature NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_assertion SIO_000772 25480889 NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_assertion wasDerivedFrom befree-2016 NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_assertion wasGeneratedBy ECO_0000203 NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245372.RA-OTf5xvd3Ix_t00E11vEkB16s20mjQUQcWzzlTuqeao130_provenance.