Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_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." NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_assertion evidence source_evidence_literature NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_assertion SIO_000772 18496125 NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_assertion wasDerivedFrom gad-20150221 NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_assertion wasGeneratedBy ECO_0000203 NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90891.RA36No4mK9WxVtRwWPsNZMq70Y50RTGaZkTNjtd1B3E3k130_provenance.