Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_assertion description "[The frequency of cytogenetic aberrations was significantly higher in the MDS cases with myelofibrosis, compared to the cases without fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_assertion evidence source_evidence_literature NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_assertion SIO_000772 1592101 NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_assertion wasDerivedFrom befree-2016 NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_assertion wasGeneratedBy ECO_0000203 NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.
- befree-2016 importedOn "2016-02-19" NP496748.RAADXO1AEiGiYbq20Ro3jZT7SKT9Tm-UtXlf0DCQO2IbE130_provenance.