Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion type Assertion NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_head.
- NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion description "[Addition of common genetic variants to traditional risk factors may be an effective method for discriminating young stroke patients at different risk of future ischemic events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_provenance.
- NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion evidence source_evidence_literature NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_provenance.
- NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion SIO_000772 19720979 NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_provenance.
- NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion wasDerivedFrom gad-20150221 NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_provenance.
- NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_assertion wasGeneratedBy ECO_0000203 NP108057.RAgHRlchMV637zAECHFDGN5EpqKP_rjxymWm2rdo8rNws130_provenance.