Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_assertion description "[Thus, ING1 mutation is very rare in breast or ovarian cancers, however, repression of ING1 expression frequently accompanies tumour development of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_assertion evidence source_evidence_literature NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_assertion SIO_000772 10498868 NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_assertion wasDerivedFrom befree-2016 NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_assertion wasGeneratedBy ECO_0000203 NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.
- befree-2016 importedOn "2016-02-19" NP263973.RAPp1u93G74yN-rNu5gE_cgTcE-sNAr5BiVTvR_eePLRU130_provenance.