Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion> ?p ?o ?g. }
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- NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion type Assertion NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_head.
- NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion description "[The G allele and AA genotype of SNP rs2834643 in RUNX1 (Pc�=�0.041-1.75�נ10(-3)), but none of the other SNPs, were associated with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_provenance.
- NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion evidence source_evidence_literature NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_provenance.
- NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion SIO_000772 23674219 NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_provenance.
- NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion wasDerivedFrom befree-20140225 NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_provenance.
- NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_assertion wasGeneratedBy ECO_0000203 NP460287.RAQXnCQbKkxBAg2_v1_K-BHR39vlBXpq-xhtgYORz4K9o130_provenance.