Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_assertion description "[Genotyping of the tumor samples in synovial sarcomas and myxoid liposarcomas revealed frequent loss of heterozygosity for XPG, mostly due to the loss of the frequent allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_assertion evidence source_evidence_literature NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_assertion SIO_000772 16646069 NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_assertion wasDerivedFrom befree-2016 NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_assertion wasGeneratedBy ECO_0000203 NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.
- befree-2016 importedOn "2016-02-19" NP547361.RAA2cFe0nrPqkqKC9ulqBqvpuR5dnF-E1YBP0_ok8xLjo130_provenance.