Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP1011730.RAydK1MD_DiSF_DWqPymdgOChy9X9N53S4D3lefYlLECk130_provenance.