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- NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_assertion type Assertion NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_head.
- NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_assertion description "[NGLY1-related disorder is a newly described autosomal recessive condition characterized by neurological, hepatic, ophthalmological findings and associated with dysmorphic features, constipation and scoliosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_provenance.
- NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_assertion evidence source_evidence_literature NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_provenance.
- NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_assertion SIO_000772 25707956 NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_provenance.
- NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_assertion wasDerivedFrom befree-2016 NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_provenance.
- NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_assertion wasGeneratedBy ECO_0000203 NP1265815.RAoqgYrLIKpTQxTbuHxoMl0rbIt0I_tmsNRSVeydCLOiE130_provenance.