Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_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." NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_assertion evidence source_evidence_literature NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_assertion SIO_000772 20932315 NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_assertion wasDerivedFrom gad-20150221 NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_assertion wasGeneratedBy ECO_0000203 NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP187057.RAwTyFmPHNW0kqkx3FX9pEw37RjYSDyN2N2_jNuK36B3w130_provenance.