Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_assertion> ?p ?o ?g. }
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- NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_assertion type Assertion NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_head.
- NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_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." NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_provenance.
- NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_assertion evidence source_evidence_literature NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_provenance.
- NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_assertion SIO_000772 14719377 NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_provenance.
- NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_assertion wasDerivedFrom befree-20140225 NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_provenance.
- NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_assertion wasGeneratedBy ECO_0000203 NP662909.RANgIx5MvszyeSsHln5mPCKN4KBzFOtnbxkFJ_L78mFq8130_provenance.