Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_assertion description "[Multiple endocrine neoplasia 2a (MEN2a) syndrome is one of the rare genetic disorder where prophylactic thyroidectomy is recommended for RET mutation carriers due to increased risk for developing MTC during lifetime.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_assertion evidence source_evidence_literature NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_assertion SIO_000772 22715565 NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_assertion wasDerivedFrom befree-2016 NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_assertion wasGeneratedBy ECO_0000203 NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.
- befree-2016 importedOn "2016-02-19" NP991569.RAwd3Wvo8Che-VZm-c36fRt1RCE0L5WEdMugkO1DerbJg130_provenance.