Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_assertion> ?p ?o ?g. }
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- NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_assertion type Assertion NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_head.
- NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_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." NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_assertion evidence source_evidence_literature NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_assertion SIO_000772 23756480 NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_assertion wasDerivedFrom befree-20140225 NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_assertion wasGeneratedBy ECO_0000203 NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.