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- NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_assertion type Assertion NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_head.
- NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_provenance.
- NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_assertion evidence source_evidence_literature NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_provenance.
- NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_assertion SIO_000772 21810944 NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_provenance.
- NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_assertion wasDerivedFrom befree-20140225 NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_provenance.
- NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_assertion wasGeneratedBy ECO_0000203 NP247392.RAsaivpTzBUJalwxlmuCu1JgS3hHgeowrJqeHjY0uyLv4130_provenance.