Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_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." NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion evidence source_evidence_literature NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion SIO_000772 20932315 NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion wasDerivedFrom gad-20130706 NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion wasGeneratedBy ECO_0000203 NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.
- gad-20130706 importedOn "2013-07-06" NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance.