Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP253457.RAAaqS9MLeexJZhYKVtjWBvgsM-juztYHBzjrVMCHe-eI130_provenance.