Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_assertion description "[Genotypes for ERLIN1, TRAPPC9, and WNK2 may prove informative for assessment of the genetic risk for intracerebral hemorrhage, and those for ITM2C and MAPKAP1 may be beneficial in assessment of the genetic risk for subarachnoid hemorrhage in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_assertion evidence source_evidence_literature NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_assertion SIO_000772 20198315 NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_assertion wasDerivedFrom gad-20150221 NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_assertion wasGeneratedBy ECO_0000203 NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP166062.RAfWZ5_A_iW3etrc98QTVtQppvTkoOn4twdEoKMsHPGzQ130_provenance.