Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion type Assertion NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_head.
- NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion description "[The highly significant association of C4AQ0 with SLE across multiple HLA haplotypes and ethnic groups, and the presence of different mechanisms leading to a C4A protein deficiency among SLE patients suggested that deficiency or low expression level of C4A protein is a primary risk factor for SLE disease susceptibility per se.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_provenance.
- NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion evidence source_evidence_literature NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_provenance.
- NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion SIO_000772 14719377 NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_provenance.
- NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion wasDerivedFrom befree-20150227 NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_provenance.
- NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_assertion wasGeneratedBy ECO_0000203 NP1013676.RAdQhAUnvmDAdXxKNnFNy4hB-co3RTtCHmW7N2rhJ0QpI130_provenance.