Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_assertion description "[As there is increasing evidence that CENPF is associated with poor prognosis in patients with primary BC, further independent studies are needed to clarify the importance of genetic variation in the CENPF gene in the clinic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_assertion evidence source_evidence_literature NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_assertion SIO_000772 19008095 NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_assertion wasDerivedFrom gad-20150221 NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_assertion wasGeneratedBy ECO_0000203 NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP133318.RAcYex7wmRhMQrjJlbmsQ4hPDVPbhzugzdVzsXzAjxrTI130_provenance.