Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_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 rar]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_assertion evidence source_evidence_literature NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_assertion SIO_000772 20932315 NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_assertion wasDerivedFrom gad-20150221 NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_assertion wasGeneratedBy ECO_0000203 NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149076.RAY4rcKDAkjlIKFAxfublgCO5I9Qr8vc2GuVdKHFgXEQU130_provenance.