Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_assertion description "[Based on a translocation finding and association to two specific alleles, the candidate gene, DYX1C1, has been proposed as the susceptibility gene for RD in 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_assertion evidence source_evidence_literature NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_assertion SIO_000772 19076634 NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_assertion wasDerivedFrom befree-2016 NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_assertion wasGeneratedBy ECO_0000203 NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.
- befree-2016 importedOn "2016-02-19" NP708907.RAiUmhBnM8-8rzRvFM0m7H4sZd6VWVjA7-Rdh_vW9cFCk130_provenance.