Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_assertion> ?p ?o ?g. }
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- NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_assertion type Assertion NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_head.
- NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_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." NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_provenance.
- NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_assertion evidence source_evidence_literature NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_provenance.
- NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_assertion SIO_000772 12891655 NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_provenance.
- NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_assertion wasDerivedFrom befree-20140225 NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_provenance.
- NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_assertion wasGeneratedBy ECO_0000203 NP745326.RAD3S-wn2ARoPJJ-oS39PR8QtY3Eqjwut_F6LXz5SjN2o130_provenance.