Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_assertion description "[Sequence alterations in CACNA1F lead to the incomplete type of CSNB (CSNB2), which can be distinguished by standard electroretinography (ERG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_assertion evidence source_evidence_literature NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_assertion SIO_000772 16960802 NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_assertion wasDerivedFrom befree-20140225 NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_assertion wasGeneratedBy ECO_0000203 NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569374.RA5a2Gi2UGKkM02-lJn3Jk7HBEcPXsg9i2RJlPKHEsYQs130_provenance.