Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_assertion wasGeneratedBy ECO_0000203 NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_assertion wasDerivedFrom befree-20140225 NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_assertion SIO_000772 22784463 NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_assertion evidence source_evidence_literature NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_assertion description "[Clinical and genetic analysis of a compound heterozygous mutation in the thyroglobulin gene in a Chinese twin family with congenital goiter and hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP328275.RAMd2D8phcTkQir2Aq55Q_Ju7NHwx1H0wmiqOQy46TLqA130_provenance.