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- NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_assertion type Assertion NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_head.
- NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_assertion wasGeneratedBy ECO_0000203 NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_provenance.
- NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_assertion wasDerivedFrom befree-2016 NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_provenance.
- NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_assertion SIO_000772 17082261 NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_provenance.
- NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_assertion evidence source_evidence_literature NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_provenance.
- NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_assertion description "[Absence of the Pax8 gene results in congenital hypothyroidism in mice, and mutations of the Pax8 gene have been associated with thyroid hypoplasia in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577511.RAwBqH_NRG15UmGfF9-KsdeXBhxDRyVb5RoYs6HN4msfo130_provenance.