Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_assertion evidence source_evidence_literature NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_assertion SIO_000772 19389850 NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_assertion wasDerivedFrom befree-20150227 NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_assertion wasGeneratedBy ECO_0000203 NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.