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- source_evidence_literature type ECO_0000212 NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_assertion description "[In addition, the percentage of individuals presenting symptoms without eosinophilia was significantly higher among homozygous carriers of ABP1 variant alleles (P<0.020) as compared with the rest of the atopic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_assertion evidence source_evidence_literature NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_assertion SIO_000772 17651147 NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_assertion wasDerivedFrom befree-20150227 NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_assertion wasGeneratedBy ECO_0000203 NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP219747.RAlr3tjGLARr_IXA_uNTnCPAHCsugtOfx7fB0iI9I-nyM130_provenance.