Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion> ?p ?o ?g. }
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- NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion type Assertion NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_head.
- NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion description "[When the simple FS patients were divided into two groups according to either having (familial) or not having a family history of FS in close relatives (sporadic), there was a significant association between IL1B -511 SNP and sporadic simple FS (p=0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_provenance.
- NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion evidence source_evidence_literature NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_provenance.
- NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion SIO_000772 19854014 NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_provenance.
- NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion wasDerivedFrom gad-20130706 NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_provenance.
- NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_assertion wasGeneratedBy ECO_0000203 NP72377.RAHejxb6fIhjr0y3SLXe9EeIVPAS9VnXSj2IXD7U-3bVM130_provenance.