Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_assertion description "[We recently characterized the mitochondrial ornithine transporter (ORNT1), the gene defective in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, a urea cycle disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_assertion evidence source_evidence_literature NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_assertion SIO_000772 12948741 NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_assertion wasDerivedFrom befree-20140225 NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_assertion wasGeneratedBy ECO_0000203 NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- befree-20140225 importedOn "2014-02-25" NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.