Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_assertion wasGeneratedBy ECO_0000203 NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_assertion wasDerivedFrom befree-20150227 NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_assertion SIO_000772 15565283 NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_assertion evidence source_evidence_literature NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.
- NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_assertion description "[We have previously described a large Chinese CMT family and assigned the locus underlying the disease (CMT2L; OMIM 608673) to chromosome 12q24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883117.RAG4nWSTUFqD9sgKKCrN6gz6WIstDFo0PO5aUgQzUHfgA130_provenance.