Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_assertion description "[To investigate the implication of SLC26A4, FOXI and KCNJ10 genes in unilateral hearing impairment associated with ipsilateral inner ear malformation (Enlargement of the vestibular aqueduct and/or Mondini dysplasia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_assertion evidence source_evidence_literature NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_assertion SIO_000772 20621367 NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_assertion wasDerivedFrom befree-2016 NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_assertion wasGeneratedBy ECO_0000203 NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.
- befree-2016 importedOn "2016-02-19" NP825106.RAqqHwVddeGfM0P-4qSnRQZmZCKpLfX1vChbvQ6F5TP3o130_provenance.