Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- befree-20150227 importedOn "2015-02-27" NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion wasGeneratedBy ECO_0000203 NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion wasDerivedFrom befree-20150227 NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion SIO_000772 23539225 NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion evidence source_evidence_literature NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.
- NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion description "[Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_provenance.