Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP800884.RAcczxenMQ8N21ljQ-lySPlIQTV4McoArTdtDwiFipeWE130_provenance.