Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_assertion description "[Deletions in 9p21.3 encompassing CDKN2A/ARF and CDKN2B were characterized as specific for the short-term recurrence group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_assertion evidence source_evidence_literature NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_assertion SIO_000772 18973227 NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_assertion wasDerivedFrom befree-20150227 NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_assertion wasGeneratedBy ECO_0000203 NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP307594.RAEdmbCDyY_aPvVc6PJXKx98Nnb4k73BQe24cHHGMHaXs130_provenance.