Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_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." NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_assertion evidence source_evidence_literature NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_assertion SIO_000772 20932315 NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_assertion wasDerivedFrom gad-20150221 NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_assertion wasGeneratedBy ECO_0000203 NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP187059.RAWFi55qEv011Q0luo0xDgMqmP_m7nxNiT1jCkGqJ-ulg130_provenance.