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- source_evidence_literature type ECO_0000212 NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_assertion description "[Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_assertion evidence source_evidence_literature NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_assertion SIO_000772 23335590 NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_assertion wasDerivedFrom befree-2016 NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_assertion wasGeneratedBy ECO_0000203 NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045463.RAntiT9iJ0KHIRJCqWJOPFoEjjRlDnoTlDHO-y11ezjR0130_provenance.