Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_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." NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_assertion evidence source_evidence_literature NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_assertion SIO_000772 20410925 NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_assertion wasDerivedFrom befree-20150227 NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_assertion wasGeneratedBy ECO_0000203 NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP749492.RAl33ZJjjJVVlL5SmqrCiIwjdWkBxL_F7kIqipxl_UYNk130_provenance.