Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_assertion description "[Selected candidate genes mapping within the aberrant genomic regions were sequenced and mutation of the TP53 gene was observed in one case in BC and of the ASXL1 gene in 6 of 41 cases in CP or BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_assertion evidence source_evidence_literature NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_assertion SIO_000772 20410925 NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_assertion wasDerivedFrom befree-20140225 NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_assertion wasGeneratedBy ECO_0000203 NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP794681.RALl1xdCNZ3XQCgMHkl43GHZCiG03acSKRv9ox-c_TXdk130_provenance.