Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_assertion description "[Lack of association of a functional single nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with susceptibility to Henoch-Sch�nlein purpura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_assertion evidence source_evidence_literature NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_assertion SIO_000772 18078626 NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_assertion wasDerivedFrom befree-20150227 NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_assertion wasGeneratedBy ECO_0000203 NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882345.RAgRg4TDRQnsA-qm8ampElUNo948CuUMY-GlglYYmiRPM130_provenance.