Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_assertion description "[For easier clinical use, these genes were re-analyzed in PBMC; qRT-PCR confirmed five novel (DNM3, IGFL2, CDO1, NEDD4L, KLHDC5) and two known genes (PLS3, TNFSF11) to be significantly overexpressed in SS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_assertion evidence source_evidence_literature NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_assertion SIO_000772 18033314 NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_assertion wasDerivedFrom befree-20150227 NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_assertion wasGeneratedBy ECO_0000203 NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP631539.RAWV_B4vhskrWVwEb9884IM5KUjPxweHH5uIzCW-lYevg130_provenance.