Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion> ?p ?o ?g. }
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- NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion type Assertion NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_head.
- NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion description "[Patients with TH deficiency suffer from progressive infantile encephalopathy dominated by motor retardation similar to a primary neuromuscular disorder, fluctuating extrapyramidal, and ocular and vegetative symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_provenance.
- NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion evidence source_evidence_literature NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_provenance.
- NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion SIO_000772 12891655 NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_provenance.
- NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion wasDerivedFrom befree-20150227 NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_provenance.
- NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_assertion wasGeneratedBy ECO_0000203 NP735291.RAU8s_10T6BlkjE9oJl6Lu_zTm8gInf6U6dVq08XXPRt0130_provenance.