Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_assertion description "[Audiometric testing revealed five (22.7%) with unrecognized sensorineural hearing loss; however, on genetic evaluation, none harbored a connexin 26 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_assertion evidence source_evidence_literature NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_assertion SIO_000772 16650419 NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_assertion wasDerivedFrom lhgdn-20090331 NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_assertion wasGeneratedBy ECO_0000203 NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199318.RApL659X8QWZJTROMDVQAMIhY48Qp4hjbng0X_Vf4UqrA130_provenance.