Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_assertion wasGeneratedBy ECO_0000203 NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_assertion wasDerivedFrom gad-20150221 NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_assertion SIO_000772 20357201 NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_assertion evidence source_evidence_literature NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.
- NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_assertion description "[The findings suggest that variants in TNF and TP53 are risk factors for POAG, whereas variants in other studied genes are not major risk factors for POAG, at least in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168786.RAUNOa3TVu1iKLXqNGAi3r7RAk_e_NUV7LWD9XCbUrfnQ130_provenance.