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- NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_assertion type Assertion NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_head.
- NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_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." NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_provenance.
- NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_assertion evidence source_evidence_literature NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_provenance.
- NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_assertion SIO_000772 17888164 NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_provenance.
- NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_assertion wasDerivedFrom befree-20140225 NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_provenance.
- NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_assertion wasGeneratedBy ECO_0000203 NP447407.RA-kjJyUJT0V_B0iJT5i4OAPCR1Derh5ggyAzK_W-l8GU130_provenance.