Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_assertion description "[Two novel mutations were identified in each of AVPR2 and AQP2 underlying Congenital Nephrogenic Diabetes Insipidus in Arab families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_assertion evidence source_evidence_literature NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_assertion SIO_000772 16845277 NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_assertion wasDerivedFrom lhgdn-20090331 NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_assertion wasGeneratedBy ECO_0000203 NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP218446.RAMyslldNeXGh--PvRkIJCmIZW91DlMNyAwHCGx2dfiKg130_provenance.