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- source_evidence_literature type ECO_0000212 NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_assertion description "[These data, combined with those indicating a similar, but even more striking, increase in rare variants found in CFI, strongly implicate complement activation in A-AMD etiopathogenesis as CFH and CFI interact to inhibit the alternative pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_assertion evidence source_evidence_literature NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_assertion SIO_000772 26501415 NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_assertion wasDerivedFrom befree-2016 NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_assertion wasGeneratedBy ECO_0000203 NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295218.RAYDd3ICmf5qd4UZF9yxNIaxAMzptU1-k_xDmd-f5314Q130_provenance.