Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_assertion description "[Our methodology allowed to statistically measure the association of a panel of SNPs with a specific phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_assertion evidence source_evidence_literature NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_assertion SIO_000772 18804983 NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_assertion wasDerivedFrom gad-20130706 NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_assertion wasGeneratedBy ECO_0000203 NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq_W_SSPF5FU130_provenance.