Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion> ?p ?o ?g. }
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- NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion type Assertion NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_head.
- NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion description "[Overall, we found 9 (13.8%) large genomic deletions or duplications: 7 out of 45 CRC patients with family history and 2 out of 20 young CRC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_provenance.
- NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion evidence source_evidence_literature NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_provenance.
- NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion SIO_000772 15949572 NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_provenance.
- NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion wasDerivedFrom befree-2016 NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_provenance.
- NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_assertion wasGeneratedBy ECO_0000203 NP498925.RAdfn5Si1vTWJiXi40vtF7Sq_RYTDpAqnEWDXONErZaVU130_provenance.