Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion> ?p ?o ?g. }
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- NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion type Assertion NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_head.
- NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion description "[Three SNP alleles in BRD2, Cx-36, and ME2 and microdeletions in 15q13.3, 15q11.2, and 16p13.11 also contribute risk to JME.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_provenance.
- NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion evidence source_evidence_literature NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_provenance.
- NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion SIO_000772 23756480 NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_provenance.
- NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion wasDerivedFrom befree-2016 NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_provenance.
- NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_assertion wasGeneratedBy ECO_0000203 NP1085037.RAEI3FRhTX7JnyaHlKYSuuf2aDWeIfyrdFoNayYrSQ6sw130_provenance.