Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_assertion description "[Alterations of known genes in PRCC include missense mutations in the MET oncogene (7q31) and rare translocations fusing TFE3 at Xp11.2 with a variety of other loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_assertion evidence source_evidence_literature NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_assertion SIO_000772 12213728 NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_assertion wasDerivedFrom befree-20140225 NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_assertion wasGeneratedBy ECO_0000203 NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP745799.RAV7Hdu_nEX1zOxcM_GIffzVUTfj88ZSynaUrFLsacZ1Y130_provenance.