Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion> ?p ?o ?g. }
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- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion type Assertion NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_head.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion description "[While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion evidence source_evidence_literature NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion SIO_000772 19507262 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion wasDerivedFrom befree-20150227 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion wasGeneratedBy ECO_0000203 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.