Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion> ?p ?o ?g. }
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- NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion type Assertion NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_head.
- NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion wasGeneratedBy ECO_0000203 NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_provenance.
- NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion wasDerivedFrom befree-20140225 NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_provenance.
- NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion SIO_000772 12511408 NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_provenance.
- NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion evidence source_evidence_literature NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_provenance.
- NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_assertion description "[Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669659.RAZ93ELW4ZrDMlnuFlUABfiCuwBMa0vaMcrZp3dsETxsE130_provenance.