Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_assertion description "[Mutations in the sodium/iodide symporter (NIS) gene as a cause for iodide transport defects and congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_assertion evidence source_evidence_literature NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_assertion SIO_000772 10403177 NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_assertion wasDerivedFrom befree-20150227 NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_assertion wasGeneratedBy ECO_0000203 NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697730.RAVZDLub32XgmlcM9rOIvqvtAa80FWNdW8ME9n9xsqMI0130_provenance.