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- NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_assertion type Assertion NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_head.
- NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_assertion wasGeneratedBy ECO_0000203 NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_provenance.
- NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_assertion wasDerivedFrom befree-2016 NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_provenance.
- NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_assertion SIO_000772 23539225 NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_provenance.
- NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_assertion evidence source_evidence_literature NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_provenance.
- NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_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." NP1064764.RAFsoeeloo5XoZqKAQMw33Yrzwj1RKWxp1Nl1v_R-K8LA130_provenance.