Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion> ?p ?o ?g. }
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- NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion type Assertion NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_head.
- NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion wasGeneratedBy ECO_0000203 NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_provenance.
- NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion wasDerivedFrom befree-20150227 NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_provenance.
- NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion SIO_000772 15008838 NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_provenance.
- NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion evidence source_evidence_literature NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_provenance.
- NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_assertion description "[We genotyped the INS-IGF2 VNTR [using the surrogate INS-23 HphI single nucleotide polymorphism (SNP)] in 823 Graves' disease (GD)/multiple sclerosis (MS) families, 1433 GD/MS patients and 837 healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1006683.RAnKxoxE5Gwknd6i1sg2SmWZx2KWnqs9jdy8mNL2wjYNI130_provenance.