Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_assertion description "[The prime candidates for genetic modifiers in CF are elements of host defence such as the TNFalpha receptor and of ion transport such as the amiloride-sensitive epithelial sodium channel ENaC, both of which are encoded side by side on 12p13 (TNFRSF1A, SCNN1A) and 16p12 (SCNN1B, SCNN1G).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_assertion evidence source_evidence_literature NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_assertion SIO_000772 16463024 NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_assertion wasDerivedFrom befree-20140225 NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_assertion wasGeneratedBy ECO_0000203 NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP907807.RAGYzDgxANIDxBT3UPUHcfAS76M0BkwgW6EHevEEwj5yY130_provenance.