Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion description "[TTC19 mutations constitute a rare cause of CIII deficiency and are associated with neurological disorders in childhood and adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion evidence source_evidence_literature NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion SIO_000772 25652355 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion wasDerivedFrom befree-2016 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion wasGeneratedBy ECO_0000203 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.