Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_assertion description "[Changes in the XRCC3 protein lead to an increase in errors in chromosome segregation due to defects in centrosomes, resulting in aneuploidy and other chromosomal aberrations, such as small increases in telomeres.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_assertion evidence source_evidence_literature NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_assertion SIO_000772 22370935 NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_assertion wasDerivedFrom befree-2016 NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_assertion wasGeneratedBy ECO_0000203 NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.
- befree-2016 importedOn "2016-02-19" NP963892.RA9wj8Bb-D9_nVXJIN5ECcKLFHzNWewpOivMf8MNoHzus130_provenance.