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DESCRIBE <http://purl.uniprot.org/SHA-384/4D7926D4447E586B5B660227FBF850E6B1D39C0B417729373C444142D019B902A34A002B516826477C930EBEF3676E32>
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http://purl.uniprot.org/SHA-384/4D7926D4447E586B5B660227FBF850E6B1D39C0B417729373C444142D019B902A34A002B516826477C930EBEF3676E32
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4D7926D4447E586B5B660227FBF850E6B1D39C0B417729373C444142D019B902A34A002B516826477C930EBEF3676E32
http://www.w3.org/2000/01/rdf-schema#comment
"A null-variant in HMCN1 (c.4162delC) has been identified in a Tunisian Jewish family with early-onset age-related macular degeneration."
xsd:string
http://purl.uniprot.org/uniprot/#_11FD4EAA82ABF98AEB4CDC3B524E57720B586E1D729B7FC6AA915C0C3C294299535D862AB157AC46B87822DBBCD73E8C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4D7926D4447E586B5B660227FBF850E6B1D39C0B417729373C444142D019B902A34A002B516826477C930EBEF3676E32
http://purl.uniprot.org/uniprot/Q96RW7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4D7926D4447E586B5B660227FBF850E6B1D39C0B417729373C444142D019B902A34A002B516826477C930EBEF3676E32
http://purl.uniprot.org/uniprot/#_Q96RW7-mappedCitation-25986072
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4D7926D4447E586B5B660227FBF850E6B1D39C0B417729373C444142D019B902A34A002B516826477C930EBEF3676E32