Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion description "[In humans, typing of the +1239A/C single nucleotide polymorphism (SNP) in the 3UTR of the Opn gene (SPP1) showed that +1239C carriers displayed higher Opn serum levels than +1239A homozygotes and a higher risk of developing autoimmune/lymphoproliferative syndrome, multiple sclerosis, and systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion evidence source_evidence_literature NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion SIO_000772 20378012 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion wasDerivedFrom befree-20140225 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion wasGeneratedBy ECO_0000203 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- befree-20140225 importedOn "2014-02-25" NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.