Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_assertion description "[Among these were 33 loci selectively methylated in neuronal but not non-neuronal chromatin from children and adults, including TSS at DPP10 (2q14.1), CNTN4 and CHL1 (3p26.3), and other neuropsychiatric susceptibility genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_assertion evidence source_evidence_literature NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_assertion SIO_000772 23185133 NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_assertion wasDerivedFrom befree-20140225 NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_assertion wasGeneratedBy ECO_0000203 NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP886541.RADpPTV_Wg__rWmQsEaIa2qNCUavhH7D3tP3r93GJaDmE130_provenance.