Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_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 t]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_assertion evidence source_evidence_literature NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_assertion SIO_000772 15730950 NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_assertion wasDerivedFrom gad-20150221 NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_assertion wasGeneratedBy ECO_0000203 NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90861.RASJe_3ATv8aCCCO8HnK8EzEAF4edQbnmE1711hxpXC-A130_provenance.