Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion type Assertion NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_head.
- NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion description "[The variant AGT Thr235 allele was more common in patients without a family history of cardiovascular disease than in patients with this risk factor (p?<?0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion evidence source_evidence_literature NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion SIO_000772 21657802 NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion wasDerivedFrom befree-2016 NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_assertion wasGeneratedBy ECO_0000203 NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.