Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_assertion description "[Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_assertion evidence source_evidence_literature NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_assertion SIO_000772 14510914 NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_assertion wasDerivedFrom befree-20140225 NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_assertion wasGeneratedBy ECO_0000203 NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP183117.RAycBGAXa9DqVFECGmLQGC15Tv3_Y3ss4l-_CO25FFZ5s130_provenance.