Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_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." NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_assertion evidence source_evidence_literature NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_assertion SIO_000772 17651147 NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_assertion wasDerivedFrom befree-20140225 NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_assertion wasGeneratedBy ECO_0000203 NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP575016.RAVFZPpGoTXd0OT4Af2WIEaJn2exl_sRzsS0dy1dRvQyw130_provenance.