Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_assertion description "[Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_assertion evidence source_evidence_literature NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_assertion SIO_000772 16684826 NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_assertion wasDerivedFrom befree-20140225 NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_assertion wasGeneratedBy ECO_0000203 NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP515301.RAUGptfPqVc_gHV-TOnvuKlf5pQ0S39n7tmMZQ9bYLVNg130_provenance.