Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_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." NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_assertion evidence source_evidence_literature NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_assertion SIO_000772 20621367 NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_assertion wasDerivedFrom befree-2016 NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_assertion wasGeneratedBy ECO_0000203 NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.
- befree-2016 importedOn "2016-02-19" NP825110.RAFUvxKQBYyOkWgRQPmOUQRWMqpGi1HfzCldD_3yOrquM130_provenance.