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- NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_assertion type Assertion NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_head.
- 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.
- NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_assertion evidence source_evidence_literature NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_provenance.
- NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_assertion SIO_000772 18309337 NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_provenance.
- NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_assertion wasDerivedFrom befree-2016 NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_provenance.
- NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_assertion wasGeneratedBy ECO_0000203 NP658030.RA6gs51APXGP0MN-p6k-Yvivw3C8HByzzeYU1x_QzFJ5k130_provenance.