Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_assertion description "[Cardiovascular diseases associated with molecular variants of individual components of renin-angiotensin system are reported to constitute inherited predisposition in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_assertion evidence source_evidence_literature NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_assertion SIO_000772 17579251 NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_assertion wasDerivedFrom befree-20140225 NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_assertion wasGeneratedBy ECO_0000203 NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP304257.RAMnF41ltY03uRExbxZ4QM-Io9-oX91FTpT5X79CC6M_Y130_provenance.