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- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion type Assertion NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_head.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion description "[Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion evidence source_evidence_literature NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion SIO_000772 17959774 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion wasDerivedFrom befree-20150227 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion wasGeneratedBy ECO_0000203 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.