Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_assertion> ?p ?o ?g. }
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- NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_assertion type Assertion NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_head.
- NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_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." NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_provenance.
- NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_assertion evidence source_evidence_literature NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_provenance.
- NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_assertion SIO_000772 16565358 NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_provenance.
- NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_assertion wasDerivedFrom befree-2016 NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_provenance.
- NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_assertion wasGeneratedBy ECO_0000203 NP542069.RAXb5Obwobo9y93UEUHuscBgDYSFRZcdylIhGAgGKsk3s130_provenance.