Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_assertion description "[Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10-bp deletion in the thyroid peroxidase (TPO) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_assertion evidence source_evidence_literature NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_assertion SIO_000772 16649969 NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_assertion wasDerivedFrom befree-20140225 NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_assertion wasGeneratedBy ECO_0000203 NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.
- befree-20140225 importedOn "2014-02-25" NP823390.RA9wx3GG7HNkaf5LedhxWKw_m-uoKkj1om0lKeZO72e00130_provenance.