Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion description "[The occurrence of thyroid carcinoma in patients with congenital hypothyroidism (CH) caused by dyshormonogenesis is very rare, and has only been reported in one patient harboring mutations in the thyroid peroxidase (TPO) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion evidence source_evidence_literature NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion SIO_000772 22435912 NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion wasDerivedFrom befree-20150227 NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion wasGeneratedBy ECO_0000203 NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance.