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DESCRIBE <http://purl.uniprot.org/SHA-384/3F24DCB8A8987DB86818F4A4E0C5385CA5E3F1789061673506107D3E18CD88018F52EAA8D53495CFE00AA32B90A69A6F>
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http://purl.uniprot.org/SHA-384/3F24DCB8A8987DB86818F4A4E0C5385CA5E3F1789061673506107D3E18CD88018F52EAA8D53495CFE00AA32B90A69A6F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/3F24DCB8A8987DB86818F4A4E0C5385CA5E3F1789061673506107D3E18CD88018F52EAA8D53495CFE00AA32B90A69A6F
http://www.w3.org/2000/01/rdf-schema#comment
"Targeted sequencing of two candidate genes SLC20A1 and SLC15A4 of the solute carrier membrane transport protein family in 200 additional patients demonstrated two further variants predicted as damaging for combined hormone deficiency."
xsd:string
http://purl.uniprot.org/uniprot/#_4490E3546B48568EBFD58902CA8A147AA491FE411D8F49AD15AB8329BC0A3449BFFD1C393DBFD117DF84309D12053DDB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/3F24DCB8A8987DB86818F4A4E0C5385CA5E3F1789061673506107D3E18CD88018F52EAA8D53495CFE00AA32B90A69A6F
http://purl.uniprot.org/uniprot/B3KVU0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/3F24DCB8A8987DB86818F4A4E0C5385CA5E3F1789061673506107D3E18CD88018F52EAA8D53495CFE00AA32B90A69A6F
http://purl.uniprot.org/uniprot/#_B3KVU0-mappedCitation-29261175
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/3F24DCB8A8987DB86818F4A4E0C5385CA5E3F1789061673506107D3E18CD88018F52EAA8D53495CFE00AA32B90A69A6F