Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_assertion description "[The result suggests that this variation has a strong association with AS in males and females. No similar reports about the association between AS and the T mutation allele have been acquired. Therefore, our hypothesis can be supported by our results on the whole and the -850C-->T mutation allele in the region on promoter of TNFalphagene is likely one of susceptible genes to AS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_assertion evidence source_evidence_literature NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_assertion SIO_000772 15730950 NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_assertion wasDerivedFrom gad-20130706 NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_assertion wasGeneratedBy ECO_0000203 NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.