Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_assertion description "[B1R gene G-->C substitution at position -699 in the promoter region and B2R gene C-->T transition at position 181 in exon 2 were genotyped in 247 family trios: offspring affected with ESRD and both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_assertion evidence source_evidence_literature NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_assertion SIO_000772 10505688 NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_assertion wasDerivedFrom befree-20150227 NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_assertion wasGeneratedBy ECO_0000203 NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP266035.RA69oHk2ncau13Hm2cZYmESClCQ88tAQsKfPBuSroDjMI130_provenance.