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- NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_assertion type Assertion NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_head.
- NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_assertion wasGeneratedBy ECO_0000203 NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_provenance.
- NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_assertion wasDerivedFrom befree-20150227 NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_provenance.
- NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_assertion SIO_000772 24390526 NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_provenance.
- NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_assertion evidence source_evidence_literature NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_provenance.
- NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_assertion description "[The patient had been diagnosed with aniridia in childhood and was found to have impaired glucose tolerance with a heterozygous PAX6 mutation 12 years prior to the current admission.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610500.RAHpwr50Rs66H9PGPDor7_mGatg0h1JkWNDMWeKLgeydg130_provenance.