Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_assertion description "[Variants of OTOF and PJVK genes in Chinese patients with auditory neuropathy spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_assertion evidence source_evidence_literature NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_assertion SIO_000772 21935370 NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_assertion wasDerivedFrom befree-20150227 NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_assertion wasGeneratedBy ECO_0000203 NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP822248.RAJ6aGcY2SHWx5TzbynsMZ95ENYod7LHh4RP7GDCEVlpM130_provenance.