Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_assertion description "[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rare causal mutations is warranted in these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_assertion evidence source_evidence_literature NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_assertion SIO_000772 20932315 NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_assertion wasDerivedFrom gad-20130706 NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_assertion wasGeneratedBy ECO_0000203 NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP85039.RAiYF7Q2mT8rWbQrjFj-akfdNlxBZhmVQhzeqXnNFwkeo130_provenance.