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- source_evidence_literature type ECO_0000212 NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_assertion description "[In addition, we report four K12 mutations in Meesmann corneal epithelial dystrophy (MCD), an autosomal dominant disorder characterized by intraepithelial microcysts and corneal epithelial fragility in which mutations in keratin 3 (K3) and K12 have recently been implicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_assertion evidence source_evidence_literature NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_assertion SIO_000772 9399908 NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_assertion wasDerivedFrom befree-20150227 NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_assertion wasGeneratedBy ECO_0000203 NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP528389.RAfqBWbE8zkhG1t3pXL6bks_hOuuhhepN3isr9eRPo_hE130_provenance.