Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_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." NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_assertion evidence source_evidence_literature NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_assertion SIO_000772 20410925 NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_assertion wasDerivedFrom befree-2016 NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_assertion wasGeneratedBy ECO_0000203 NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.
- befree-2016 importedOn "2016-02-19" NP807627.RAjoRJJP53rShXmnq1sJBN8oWPWgg1ZKNZcJ1xtp8C7Ig130_provenance.