Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_assertion description "[Investigating all common variants in IL1A, IL1B, IL1RN,IL6 and IL10 genes revealed a statistically significant association (rs452204 p(empirical) = 0.02) with one IL1RN variant and ESRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_assertion evidence source_evidence_literature NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_assertion SIO_000772 20551628 NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_assertion wasDerivedFrom befree-2016 NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_assertion wasGeneratedBy ECO_0000203 NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.
- befree-2016 importedOn "2016-02-19" NP819134.RANQCVCvum3GS6O1I-VjyEXVObENt4s4lgCO5G7PvV7HE130_provenance.