Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion> ?p ?o ?g. }
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- NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion type Assertion NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_head.
- NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion description "[This study demonstrates evidence of a novel locus SPG38 for Silver syndrome (SS) and suggests that genetic defects in SPG4 might lead to broad clinical features overlapped with those of SS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion evidence source_evidence_literature NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion SIO_000772 18401025 NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion wasDerivedFrom befree-20150227 NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_assertion wasGeneratedBy ECO_0000203 NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.