Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion> ?p ?o ?g. }
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- NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion type Assertion NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_head.
- NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion wasGeneratedBy ECO_0000203 NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_provenance.
- NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion wasDerivedFrom befree-20140225 NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_provenance.
- NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion SIO_000772 21035104 NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_provenance.
- NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion evidence source_evidence_literature NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_provenance.
- NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_assertion description "[Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531835.RAcjy5lW_pdr6JoUU239eDRXrQ2Qy6elQeZQSU_-1eNX8130_provenance.