Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_assertion description "[Two cases, twins, affected by congenital nephrogenic diabetes insipidus (CNDI) with a high daily volume of dilute urine excretion and periods of compensatory high levels of antidiuretic hormone (ADH) simultaneously developed a fluctuating Meni�re-type hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_assertion evidence source_evidence_literature NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_assertion SIO_000772 1443085 NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_assertion wasDerivedFrom befree-20140225 NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_assertion wasGeneratedBy ECO_0000203 NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP419352.RAmk4jnCkhFNUjHUPNeVR05ler8UV5iVtmJMe6E03tfiE130_provenance.