Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion> ?p ?o ?g. }
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- NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion type Assertion NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_head.
- NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion description "[We genotyped a panel of 1,472 SNPs to capture the common genomic variation across the 3.44 megabase (Mb) classic MHC region in 10,576 DNA samples derived from patients with systemic lupus erythematosus, Crohn's disease, ulcerative colitis, rheumatoid arthritis, myasthenia gravis, selective IgA deficiency, multiple sclerosis, and appropriate control samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance.
- NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion evidence source_evidence_literature NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance.
- NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion SIO_000772 19846760 NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance.
- NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion wasDerivedFrom befree-2016 NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance.
- NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion wasGeneratedBy ECO_0000203 NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance.