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- source_evidence_literature type ECO_0000212 NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP900684.RAjcmz9qnHzcBjkmFep8CmUMtJrxBXXwfTmJ5pfo7M2Hk130_provenance.