Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_assertion description "[Four of nine informative fetal rhabdomyomas and embryonal rhabdomyosarcomas showed loss of heterozygosity (LOH) in the PTCH region with two of these (one fetal rhabdomyoma and one embryonal rhabdomyosarcoma) also showing LOH in the SUFU region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_assertion evidence source_evidence_literature NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_assertion SIO_000772 16294371 NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_assertion wasDerivedFrom befree-20140225 NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_assertion wasGeneratedBy ECO_0000203 NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP818717.RA3iMVIr5WlUxQu-sK1_Tg7mg47J4pvBDUcFPDgF369O0130_provenance.