Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_assertion description "[Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_assertion evidence source_evidence_literature NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_assertion SIO_000772 20932283 NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_assertion wasDerivedFrom befree-20150227 NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_assertion wasGeneratedBy ECO_0000203 NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP900883.RAVGLy8aBFQSlSrnIyGfM6_ouq9mAzDQyYIDjN6ljXNyY130_provenance.