Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion type Assertion NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_head.
- NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion wasGeneratedBy ECO_0000203 NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion wasDerivedFrom befree-20150227 NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion SIO_000772 1311149 NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion evidence source_evidence_literature NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_assertion description "[Gelsolin gene mutation--at codon 187--in familial amyloidosis, Finnish: DNA-diagnostic assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.