Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_assertion description "[Complete deficiencies of complement components C4A and C4B, albeit rare in human populations, are among the strongest genetic risk factors for SLE or lupus-like disease, across HLA haplotypes and racial backgrounds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_assertion evidence source_evidence_literature NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_assertion SIO_000772 14719377 NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_assertion wasDerivedFrom befree-20140225 NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_assertion wasGeneratedBy ECO_0000203 NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP854816.RAYZRSx3OHbN4J0UJ3Guy0dp_zbwnsuCbuo396cKWq2UQ130_provenance.