Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_assertion evidence source_evidence_literature NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_assertion SIO_000772 20801516 NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_assertion wasDerivedFrom gad-20150221 NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_assertion wasGeneratedBy ECO_0000203 NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP147305.RARjJ8E13unkaibePXkyvPJlCg8h5amKTg-Km76C3cIpA130_provenance.