Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_assertion description "[The incidence of loss of heterozygosity at D3S643 and at IFNA were higher in SCC than in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_assertion evidence source_evidence_literature NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_assertion SIO_000772 10697627 NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_assertion wasDerivedFrom befree-20150227 NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_assertion wasGeneratedBy ECO_0000203 NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.
- befree-20150227 importedOn "2015-02-27" NP478317.RAVjJT1R0sri3iPjg28T-dy2Ir_9QtZKzMYSFle0yDSes130_provenance.