Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion> ?p ?o ?g. }
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- NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion type Assertion NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_head.
- NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion wasGeneratedBy ECO_0000203 NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_provenance.
- NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion wasDerivedFrom befree-20140225 NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_provenance.
- NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion SIO_000772 12483741 NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_provenance.
- NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion evidence source_evidence_literature NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_provenance.
- NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_assertion description "[We investigated whether patients with this disorder have mutations in CIAS1, the gene which causes Muckle-Wells syndrome and familial cold autoinflammatory syndrome, two dominantly inherited disorders with some similarities to NOMID/CINCA syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334042.RAKBpc3JjoBHtiLbcoge6DXGGR7-GfrqP5ctBRjQe1sV8130_provenance.