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- source_evidence_literature type ECO_0000212 NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_assertion description "[In addition, six previously reported (p.R48G, p.A119S, p.V432L, p.D449D, p.N453S, and 372-12C>T in intron 1) and four novel (p.V395V, p.P400P, p.V518A, and c.2016C>G in the 3'-UTR) single nucleotide polymorphism (SNPs) were also observed in POAG patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_assertion evidence source_evidence_literature NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_assertion SIO_000772 16688110 NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_assertion wasDerivedFrom befree-20140225 NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_assertion wasGeneratedBy ECO_0000203 NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP710003.RA2e9c4_x8dIeHyBjJp_Y0VHqxZM4EIy8EhwhKt3TzCmo130_provenance.