Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_assertion description "[In conclusion, this study shows that the KTS splice site mutation is not specific for Frasier syndrome, but that it can also be found in DDS and in a normal female (XX) with FSGS, a woman who achieved normal pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_assertion evidence source_evidence_literature NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_assertion SIO_000772 10505700 NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_assertion wasDerivedFrom befree-2016 NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_assertion wasGeneratedBy ECO_0000203 NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.
- befree-2016 importedOn "2016-02-19" NP264484.RAHOwWPYn4KJjzC8ODtcWYaaZG8LP9r2egHa_e9BaNb80130_provenance.