Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion> ?p ?o ?g. }
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- NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion type Assertion NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_head.
- NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion description "[A cohort of 19 families (n=170) with a history of idiopathic CP (ICP) was screened for mutations within the CASR gene; 104 members of that cohort had a mutation (N34S) within the SPINK1 gene and 66 of those were suffering from CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion evidence source_evidence_literature NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion SIO_000772 16497624 NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion wasDerivedFrom befree-20140225 NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_assertion wasGeneratedBy ECO_0000203 NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.