Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_assertion description "[The inverse correlation of RB and p16INK4 expression and the absence of p16INK4 inactivation in RB (-/-) SCLC lines (0/48) confirms a common p16INK4/RB growth suppressor pathway in human cancers and provides evidence that p16INK4, and not an adjacent gene on chromosome 9p, is a specific target for mutational events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_assertion evidence source_evidence_literature NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_assertion SIO_000772 7936665 NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_assertion wasDerivedFrom befree-2016 NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_assertion wasGeneratedBy ECO_0000203 NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327557.RATiM1u7Sr3lUfFH1wEl3gON0HAIrOuKGYsMme0pKhRII130_provenance.