Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_assertion description "[To investigate possible consequences of this genetic alteration for tumor development, we conditionally expressed p16(INK4A) in the T-cell acute lymphoblastic leukemia line CCRF-CEM, which carries a homozygous deletion of this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_assertion evidence source_evidence_literature NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_assertion SIO_000772 11441822 NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_assertion wasDerivedFrom befree-2016 NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_assertion wasGeneratedBy ECO_0000203 NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.
- befree-2016 importedOn "2016-02-19" NP323037.RA4nwWzIK414ICOtNX1iJApzfiZrD78HqVLALi9TjynVg130_provenance.