Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP436933.RABH1223UKs6CNPJAIRoGfRBHocyzagSy0tz_clf84eGA130_provenance.
- 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.