Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_assertion description "[Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_assertion evidence source_evidence_literature NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_assertion SIO_000772 22057234 NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_assertion wasDerivedFrom befree-20150227 NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_assertion wasGeneratedBy ECO_0000203 NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475311.RAkVnwuh3fERJOHeVQ03HYOCkTIjDXXiRcpfyE8NSkgI8130_provenance.