Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_assertion description "[To our knowledge, this is the first report of successful simultaneous detection of multiple genetic polymorphisms with point mutations using ASPCR-MP or multiple genetic polymorphisms with large structural alterations using stepdown PCR. In conclusion, AS]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_assertion evidence source_evidence_literature NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_assertion SIO_000772 15691505 NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_assertion wasDerivedFrom gad-20150221 NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_assertion wasGeneratedBy ECO_0000203 NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP54938.RAEBnFY6w6FY9vkuQ7L2w9GqHVtJ9BXPdYGU1NBJlCcYo130_provenance.