Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_assertion> ?p ?o ?g. }
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- NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_assertion type Assertion NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_head.
- NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_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." NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_provenance.
- NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_assertion evidence source_evidence_curated NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_provenance.
- NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_assertion SIO_000772 16565358 NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_provenance.
- NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_assertion wasDerivedFrom ctd_human-20150221 NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_provenance.
- NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_assertion wasGeneratedBy ECO_0000218 NP25858.RAvGVpJIkwz_-R-mg_BYQVrBFZfnV3jHosOV-RGT72L2M130_provenance.