Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_assertion description "[Its human homologue, RAE28, is located on chromosome 12p13, which frequently is associated with chromosomal abnormalities and loss of heterozygosity in patients with hematologic malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_assertion evidence source_evidence_literature NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_assertion SIO_000772 11164110 NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_assertion wasDerivedFrom befree-2016 NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_assertion wasGeneratedBy ECO_0000203 NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP306184.RAl-NI0PSsSmPSImW9JTDlRRGNZVDNq1MQJfE2dFi07UQ130_provenance.