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- NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion type Assertion NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_head.
- NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion description "[The persistent mA1/4llerian duct syndrome, characterized by the lack of regression of mA1/4llerian derivatives, uterus and tubes in otherwise normally masculinized males, is a genetically transmitted disorder implicating either anti-mA1/4llerian hormone (AMH), a member of the transforming growth factor-beta superfamily, or its type II receptor, a serine/threonine kinase homologous to the receptors of other members of the transforming growth factor-beta superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance.
- NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion evidence source_evidence_curated NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance.
- NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion SIO_000772 8872466 NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance.
- NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion wasDerivedFrom uniprot-20150221 NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance.
- NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion wasGeneratedBy ECO_0000218 NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance.