Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP354484.RANaGJVdCW_C-wRGNsIHGJodAd18_Y0sKmFzX_4K5upxc130_provenance.