Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion wasGeneratedBy ECO_0000203 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion wasDerivedFrom befree-20140225 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion SIO_000772 18528812 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion evidence source_evidence_literature NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion description "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.