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- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion type Assertion NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_head.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion description "[Also studied were two siblings who were homozygous for the PITX3 mutation who had microphthalmia and significant neurologic impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion evidence source_evidence_literature NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion SIO_000772 16565358 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion wasDerivedFrom befree-20150227 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion wasGeneratedBy ECO_0000203 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.