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- source_evidence_literature type ECO_0000212 NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_assertion description "[These findings suggest that the 20210A prothrombin allele represents an inherited risk factor for acute coronary syndrome among patients who have limited extent of coronary disease at angiography or who lack major metabolic and acquired risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_assertion evidence source_evidence_literature NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_assertion SIO_000772 11741359 NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_assertion wasDerivedFrom befree-2016 NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_assertion wasGeneratedBy ECO_0000203 NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.
- befree-2016 importedOn "2016-02-19" NP338713.RAakoF21INw10jKt6QytSdHgiett1YX_AzsCpXbG-iXO8130_provenance.