Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_assertion description "[Although borderline support for association between polymorphisms in TLR genes and AMD was reported for some cohorts, these initial observations of coding SNPs in TLR3, TLR4, and TLR7 were not replicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_assertion evidence source_evidence_literature NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_assertion SIO_000772 18385087 NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_assertion wasDerivedFrom gad-20130706 NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_assertion wasGeneratedBy ECO_0000203 NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP80706.RA2FW8nFpsyQ_s54UCLpxV4Y51erfVDWJQNQ2q-T76HMQ130_provenance.