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- source_evidence_literature type ECO_0000212 NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_assertion description "[NIS mutations are found in congenital hypothyroidism, and potential defects in the NIS gene, its expression, or function of the NIS protein are currently under investigation in various thyroid diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_assertion evidence source_evidence_literature NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_assertion SIO_000772 9865544 NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_assertion wasDerivedFrom befree-20150227 NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_assertion wasGeneratedBy ECO_0000203 NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697729.RAf8gDR8RSQ_hfdJZBfH32DBhi-yemiqkrbPr4fDOTAdA130_provenance.