Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_assertion description "[The variability of cystic fibrosis lung disease and the variable expressivity of mild CFTR alleles complicate genetic counseling for this autosomal recessive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_assertion evidence source_evidence_literature NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_assertion SIO_000772 19092437 NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_assertion wasDerivedFrom befree-20140225 NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_assertion wasGeneratedBy ECO_0000203 NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775306.RAdj93dR7Sr72UXNc_siMZVgueCrO2CJTFq_0zpCoSsGQ130_provenance.