Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_assertion description "[Present and earlier data on 23 PAs showed that tumors with the highest frequency of abnormal karyotypes revealed by cytogenetics and/or interphase FISH were PRL (78%), followed by NFPA (26%) and GH (18%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_assertion evidence source_evidence_literature NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_assertion SIO_000772 10760821 NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_assertion wasDerivedFrom befree-2016 NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_assertion wasGeneratedBy ECO_0000203 NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.
- befree-2016 importedOn "2016-02-19" NP280796.RAn4Y1PjdKkNbkCUDSgJT9OGGIInlUL-NopwbdqiwekwU130_provenance.