Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_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." NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_assertion evidence source_evidence_literature NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_assertion SIO_000772 20410925 NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_assertion wasDerivedFrom befree-2016 NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_assertion wasGeneratedBy ECO_0000203 NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.
- befree-2016 importedOn "2016-02-19" NP807625.RA_Eu0jFy1UHwahgl4owhEXDeaa7Y9PN8xwvAZpgv-YIY130_provenance.