Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_assertion description "[Mutations in the TPO gene are common in congenital hypothyroidism, and there are also signs of the implication of TPO in thyroid cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_assertion evidence source_evidence_literature NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_assertion SIO_000772 23754668 NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_assertion wasDerivedFrom befree-2016 NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_assertion wasGeneratedBy ECO_0000203 NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1084836.RAj8fgkRgUNujW28FGW2Mv3Kjn55QJuvzlmCz53FxZUSw130_provenance.