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DESCRIBE <http://purl.uniprot.org/SHA-384/17ECFB354CDCDB195E524FD3DC5A2306254B9FF098908E64F8000CDA7B338AEE86BD288EA54467695C7CBE4CA7AEAAE1>
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http://purl.uniprot.org/SHA-384/17ECFB354CDCDB195E524FD3DC5A2306254B9FF098908E64F8000CDA7B338AEE86BD288EA54467695C7CBE4CA7AEAAE1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/17ECFB354CDCDB195E524FD3DC5A2306254B9FF098908E64F8000CDA7B338AEE86BD288EA54467695C7CBE4CA7AEAAE1
http://www.w3.org/2000/01/rdf-schema#comment
"A c.683C>T (p.Thr228Met) mutation in FNBP4 was found as a primary candidate to microphthalmia with limb anomalies"
xsd:string
http://purl.uniprot.org/uniprot/#_624EF1DD8AE10A6F90188CDBE44F402CE89848335EFA2997A2E1D39787735A77EA9AB05BDFAE7B2234D5B55AA0C4D2D8
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/17ECFB354CDCDB195E524FD3DC5A2306254B9FF098908E64F8000CDA7B338AEE86BD288EA54467695C7CBE4CA7AEAAE1
http://purl.uniprot.org/uniprot/B3KNP0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/17ECFB354CDCDB195E524FD3DC5A2306254B9FF098908E64F8000CDA7B338AEE86BD288EA54467695C7CBE4CA7AEAAE1
http://purl.uniprot.org/uniprot/#_B3KNP0-mappedCitation-23703728
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/17ECFB354CDCDB195E524FD3DC5A2306254B9FF098908E64F8000CDA7B338AEE86BD288EA54467695C7CBE4CA7AEAAE1