Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_assertion description "[The cellular variant of congenital mesoblastic nephroma (but not the classic variant) has been shown to bear the same t(12;15)(p13;q25) and ETV6-NTRK3 gene fusion as infantile fibrosarcoma, a tumor with which it shares morphologic and clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_assertion evidence source_evidence_literature NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_assertion SIO_000772 12973047 NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_assertion wasDerivedFrom befree-20150227 NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_assertion wasGeneratedBy ECO_0000203 NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387291.RAki8X3OGRjGSMo9iDnOGgPV4DOWllUn1M6te97TSsuhE130_provenance.