Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_assertion wasGeneratedBy ECO_0000203 NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_assertion wasDerivedFrom befree-20150227 NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_assertion SIO_000772 25146893 NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_assertion evidence source_evidence_literature NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.
- NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_assertion description "[Loss of function mutations in TSHR, PAX8, NKX2.1, NKX2.5 and FOXE1 genes are responsible for some forms of inherited congenital hypothyroidism, with or without hypoplastic thyroid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404846.RAywrVIzAPNamDzwiWOCc-ujqLVG6s1xibXl5yUFoS7B0130_provenance.