Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_assertion description "[The overall results supported that the genetic variants in the contractile pathway of VSMC could contribute to hypertension risk independently or in an interactive manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_assertion evidence source_evidence_literature NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_assertion SIO_000772 18496125 NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_assertion wasDerivedFrom gad-20130706 NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_assertion wasGeneratedBy ECO_0000203 NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130_provenance.