Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_assertion> ?p ?o ?g. }
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- NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_assertion type Assertion NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_head.
- NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_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." NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_provenance.
- NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_assertion evidence source_evidence_literature NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_provenance.
- NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_assertion SIO_000772 23756480 NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_provenance.
- NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_assertion wasDerivedFrom befree-20150227 NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_provenance.
- NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_assertion wasGeneratedBy ECO_0000203 NP929562.RAq05DD-HZoTL4SCMwW9UNE8YjowlpDSpvP2-cWodmaJY130_provenance.