Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_assertion description "[Mutations in the CFTR gene lead to cystic fibrosis, the most frequent genetic disease in the Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_assertion evidence source_evidence_literature NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_assertion SIO_000772 23072488 NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_assertion wasDerivedFrom befree-20150227 NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_assertion wasGeneratedBy ECO_0000203 NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP311206.RAo-kOdYV3vDflGEtLEj_XRTqbUoVbzTvVY3KEytwboSM130_provenance.