Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_assertion description "[The small effect sizes may limit the prognostic, diagnostic, and therapeutic use of SNP markers such as those in MAMDC1. However, the present study demonstrates the potential of a GWAS to discover potentially important pathogenic pathways for which clinic]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_assertion evidence source_evidence_literature NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_assertion SIO_000772 18762592 NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_assertion wasDerivedFrom gad-20150221 NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_assertion wasGeneratedBy ECO_0000203 NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP158082.RAAQjdBo9ePQQHwcXyncxDYGKIC1LP9phAvQujSn0W_8c130_provenance.