Matches in Nanopublications for { ?s ?p "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP650948.RAdwtqGew1BKZ7yZaeCHhqmswmEj4vy7hBQUT4QrJzkq8130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650948.RAdwtqGew1BKZ7yZaeCHhqmswmEj4vy7hBQUT4QrJzkq8130_provenance.
- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_provenance.
- NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- NP522840.RA7gsMMkqIHe6-4944eoqXoMIbNCEG2uik6o1sGlcok7k130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522840.RA7gsMMkqIHe6-4944eoqXoMIbNCEG2uik6o1sGlcok7k130_provenance.
- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_provenance.