Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_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." NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_assertion evidence source_evidence_literature NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_assertion SIO_000772 20932315 NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_assertion wasDerivedFrom gad-20130706 NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_assertion wasGeneratedBy ECO_0000203 NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP89992.RAiWeoqHaLpfUL_SdehQXcXBGSe1vZ4DBJ1s8DoYuRvb8130_provenance.