Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_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." NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_assertion evidence source_evidence_literature NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_assertion SIO_000772 17651147 NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_assertion wasDerivedFrom befree-2016 NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_assertion wasGeneratedBy ECO_0000203 NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.
- befree-2016 importedOn "2016-02-19" NP621461.RAunGX2LTBVMj6-h92t75LfMORob-PL-I08W3ffwcAQz4130_provenance.