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- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion type Assertion NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_head.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion wasGeneratedBy ECO_0000203 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion wasDerivedFrom befree-2016 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion SIO_000772 16272056 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion evidence source_evidence_literature NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion description "[Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) have recently been discovered to cause a form of autosomal dominant retinitis pigmentosa (adRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.