Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_assertion description "[Dominantly inherited cataracts with differing clinical features were found in two families carrying different point mutations in the gene encoding lens water channel protein AQP0 (major intrinsic protein, MIP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_assertion evidence source_evidence_literature NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_assertion SIO_000772 11001937 NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_assertion wasDerivedFrom befree-2016 NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_assertion wasGeneratedBy ECO_0000203 NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.
- befree-2016 importedOn "2016-02-19" NP295870.RArf1lpVYy9aj7km-CiJLugWLxeEE2FimNJ5x2TPfYMiA130_provenance.