Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_assertion description "[WG patients without ESRD had a higher frequency of the IL10 GCC/ACC promotor genotype (OR = 0.13) and long CTLA4 (AT)(n) repeats (OR = 0.4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_assertion evidence source_evidence_literature NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_assertion SIO_000772 15708894 NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_assertion wasDerivedFrom befree-2016 NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_assertion wasGeneratedBy ECO_0000203 NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.
- befree-2016 importedOn "2016-02-19" NP480708.RAgV6l8KD2zld8yE2ISQN8r4HrPmktdWwp85PkCDNLnww130_provenance.