Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_assertion description "[Loss of p16INK4A expression was observed in three cases (13.6%) of ACC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_assertion evidence source_evidence_literature NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_assertion SIO_000772 10928172 NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_assertion wasDerivedFrom befree-20140225 NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_assertion wasGeneratedBy ECO_0000203 NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP695548.RAgqrt_iNXLo44Ct_DW-4oHlWF_SktVOO1XpPAqzx7lcA130_provenance.