Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion> ?p ?o ?g. }
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- NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion type Assertion NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_head.
- NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion description "[Second, counseling to parents of affected children should be cautious because although the theoretical risk of inheriting the ARSE mutation is 50% for every male child of a carrier mother, it is not possible to determine whether he will develop features of CDPX1 and the eventual severity of symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion evidence source_evidence_literature NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion SIO_000772 19839041 NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion wasDerivedFrom befree-20150227 NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_assertion wasGeneratedBy ECO_0000203 NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.