Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_assertion description "[We carried out a case-control study to test for association between AMD and single nucleotide polymorphisms (SNPs) spanning the genes encoding complement factor P (CFP, properdin), CD46 (membrane cofactor protein, MCP), CD55 (decay accelerating factor, DAF) and CD59 (protectin).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_assertion evidence source_evidence_literature NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_assertion SIO_000772 22024702 NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_assertion wasDerivedFrom befree-20140225 NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_assertion wasGeneratedBy ECO_0000203 NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449501.RAAzcKKaY4F2JgxSXwWAyI2KWRvpcp8QbSBmjHhrerP9o130_provenance.