Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_assertion description "[In contrast, we report a statistically significant association of common variants in the ABCA4 gene with retinal disease, assessed by a score-based variance-component test (PSKAT = 0.0055).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_assertion evidence source_evidence_literature NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_assertion SIO_000772 25884411 NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_assertion wasDerivedFrom befree-2016 NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_assertion wasGeneratedBy ECO_0000203 NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1278681.RAf3PYlS2wnlAK5njNk9SejrJ3eAcYF5EBV-g8k95epMw130_provenance.