Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion> ?p ?o ?g. }
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- NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_assertion type Assertion NP609262.RAzNXxeLv-tr6P_GX_2yl7hQedrBG2XHYI9px4AsqY9ek130_head.
- 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.