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- NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_assertion type Assertion NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_head.
- NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_assertion description "[Human patients with point mutations in PITX3 demonstrate congenital cataracts along with anterior segment defects in some cases when one allele is affected and microphthalmia with brain malformations when both copies are mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_provenance.
- NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_assertion evidence source_evidence_literature NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_provenance.
- NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_assertion SIO_000772 17888164 NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_provenance.
- NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_assertion wasDerivedFrom befree-20150227 NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_provenance.
- NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_assertion wasGeneratedBy ECO_0000203 NP626566.RAbLTs0qy-0EFTqsJmZpwTQfQazHSdTi8jAlDl9uKrPNc130_provenance.