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- NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_assertion type Assertion NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_head.
- NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_assertion wasGeneratedBy ECO_0000203 NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_provenance.
- NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_assertion wasDerivedFrom lhgdn-20090331 NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_provenance.
- NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_assertion SIO_000772 15001591 NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_provenance.
- NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_assertion evidence source_evidence_literature NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_provenance.
- NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_assertion description "[six novel and two recurrent intragenic KAL1 mutations in seven familial and four sporadic male cases of Kallmann syndrome]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215506.RAm1dR04U-JNb9ra5a1e2Ygwh4dbhk2VYtmGIiOxEXPHg130_provenance.