Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_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." NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_assertion evidence source_evidence_literature NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_assertion SIO_000772 11001937 NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_assertion wasDerivedFrom befree-2016 NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_assertion wasGeneratedBy ECO_0000203 NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.
- befree-2016 importedOn "2016-02-19" NP295873.RAFKc3EPjqewZYTTviR0u304ty-HBT3wn5s_LJPSQlaLw130_provenance.