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About:
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
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wikibase:Item
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scientific article published on 01 September 1999
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rdf:type
Item
description
wetenschappelijk artikel
(nl)
наукова стаття, опублікована у вересні 1999
(uk)
im September 1999 veröffentlichter wissenschaftlicher Artikel
(de)
artículu científicu espublizáu en setiembre de 1999
(ast)
scientific article published on 01 September 1999
(en)
publication date
wds:Q78126999-E19FE465-D92D-4EED-ACC2-3195677B639F
publication date
1999-09-01 00:00:00Z
(
xsd:dateTime
)
exact match
wds:Q78126999-3DABBB33-A766-42F5-8E09-E2370E948FFE
exact match
https://scigraph.springernature.com/pub.10.1007/s004170050301
author name string
wds:Q78126999-01CFA5AF-3740-44CC-B223-AEDDFBA59B76
wds:Q78126999-16864728-B609-47CC-934B-DCC6542D233D
wds:Q78126999-35F9DA92-464D-4340-B88C-5118EBC321C5
wds:Q78126999-86FCED6F-5E60-44A3-9137-C236DEB71985
wds:Q78126999-94C50B0B-0588-44A9-BDAA-4162CD298E7A
wds:Q78126999-96D9AAE7-3F50-4316-8D0E-297A8B6B8BA5
wds:Q78126999-D3E26E53-493F-44AE-911C-DBC5782D46ED
author name string
B Wissinger
U Kellner
M H Foerster
H Kraus
H Thieme
M Christ-Adler
C Jandeck
rdfs:label
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(en)
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(nl)
skos:prefLabel
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(en)
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(nl)
name
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(en)
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(nl)
title
wds:Q78126999-FDE6BFE4-7FFB-4E3C-9514-A3F1A6FB544A
title
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
(en)
page(s)
wds:Q78126999-D7A79072-CA91-4FB8-9189-E2575416C708
page(s)
714-719
instance of
wds:Q78126999-5D854E9A-F06E-41C5-B39A-4C69796AB42E
instance of
scholarly article
main subject
wds:Q78126999-9E5393A9-91A5-4268-8038-19B161F5DDD7
main subject
hereditary optic neuropathy
PubMed ID
wds:Q78126999-3158EAFF-6E77-4786-B4EE-E0609B22E3AC
PubMed ID
http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10447644
PubMed ID
10447644
published in
wds:Q78126999-3AB9726C-3546-49C8-A4A2-FFFF110C27EB
published in
Graefe's Archive for Clinical and Experimental Ophthalmology
issue
wds:Q78126999-566FE05A-EAEF-4887-A875-0FE7DFDEF986
volume
wds:Q78126999-7EAEEB64-2B49-4166-82B4-87F849BF0B23
issue
9
volume
237
DOI
wds:Q78126999-BE46F0BE-C638-40F8-9296-79E664991FDA
DOI
http://dx.doi.org/10.1007/S004170050301
DOI
10.1007/S004170050301
Dimensions Publication ID
wds:Q78126999-40BB3A78-9221-4464-A779-4485F43F149E
Dimensions Publication ID
1043527092
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q78126999
is
cites work
of
Chapter 4 Leber's Hereditary Optic Neuropathy
Analysis of Visual Field Defects Obtained with Semiautomated Kinetic Perimetry in Patients with Leber Hereditary Optic Neuropathy.
Phosphorylated neurofilament heavy chain is a marker of neurodegeneration in Leber hereditary optic neuropathy (LHON)
Leber's hereditary optic neuropathy: a case report
is
cites work
of
wds:Q55092284-B761354C-3F5B-4AE7-A319-DE5E2407F9F1
wds:Q57721287-04B46105-DEC4-4D83-BAC2-7C7BC622F883
wds:Q81731818-335F6E46-9279-4CA6-BF9C-2343FEBA914D
wds:Q37021025-FE66B4B2-F5E6-4FDC-9567-6365C7615C1F
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