Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_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." NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_assertion evidence source_evidence_literature NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_assertion SIO_000772 12891655 NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_assertion wasDerivedFrom befree-2016 NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_assertion wasGeneratedBy ECO_0000203 NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.
- befree-2016 importedOn "2016-02-19" NP403881.RAFOFlgfq0EF2EvSMe_tx7nd7ryAKObq16f5jw85sgnCI130_provenance.