Sha256: 84b7ef07e47f4364e5548d4946dfd79d9ab689be14a347010cb1f4a2889a3a91
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Versions: 4
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Contents
{ "resourceType": "Sequence", "id": "example-pgx-1", "text": { "status": "generated", "div": "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: example-pgx-1</p><p><b>type</b>: DNA</p><p><b>coordinateSystem</b>: 0</p><p><b>patient</b>: <a>Patient/example</a></p><h3>ReferenceSeqs</h3><table><tr><td>-</td><td><b>ReferenceSeqId</b></td><td><b>Strand</b></td><td><b>WindowStart</b></td><td><b>WindowEnd</b></td></tr><tr><td>*</td><td>NG_007726.3 <span>(Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NG_007726.3' = 'NG_007726.3)</span></td><td>1</td><td>55227970</td><td>55227980</td></tr></table><h3>Variants</h3><table><tr><td>-</td><td><b>Start</b></td><td><b>End</b></td><td><b>ObservedAllele</b></td><td><b>ReferenceAllele</b></td><td><b>VariantPointer</b></td></tr><tr><td>*</td><td>55227976</td><td>55227977</td><td>G</td><td>T</td><td><a>Target Haplotype Observation</a></td></tr></table></div>" }, "type": "DNA", "coordinateSystem": 0, "patient": { "reference": "Patient/example" }, "referenceSeq": { "referenceSeqId": { "coding": [ { "system": "http://www.ncbi.nlm.nih.gov/nuccore", "code": "NG_007726.3" } ] }, "strand": 1, "windowStart": 55227970, "windowEnd": 55227980 }, "variant": [ { "start": 55227976, "end": 55227977, "observedAllele": "G", "referenceAllele": "T", "variantPointer": { "reference": "Observation/example-haplotype1", "display": "Target Haplotype Observation" } } ] }
Version data entries
4 entries across 4 versions & 1 rubygems