Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_assertion evidence source_evidence_literature NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_assertion SIO_000772 10554356 NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_assertion wasDerivedFrom befree-20140225 NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_assertion wasGeneratedBy ECO_0000203 NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- befree-20140225 importedOn "2014-02-25" NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.