Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_assertion description "[the AGTR1 A1166C and the NOS3 G894T polymorphisms are associated with silent white matter lesions in the subcortical area in essential hypertension]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_assertion evidence source_evidence_literature NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_assertion SIO_000772 16109907 NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_assertion wasDerivedFrom lhgdn-20090331 NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_assertion wasGeneratedBy ECO_0000203 NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP186263.RAm12-MYR-UFo0CdIRahwgV76noN3RGHP-UA6Uhc1izmw130_provenance.