Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_assertion description "[This study revealed that e.g., the t(12;21) [ETV6-RUNX1] subtype of ALL and the t(15;17) [PML-RARA] subtype of AML had transcriptional programs similar to those in normal Pro-B cells and promyelocytes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_assertion evidence source_evidence_literature NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_assertion SIO_000772 20211010 NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_assertion wasDerivedFrom befree-20140225 NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_assertion wasGeneratedBy ECO_0000203 NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP255489.RAdqNBRrUMLZ8tIdBFQ_wV1Qa-qZ2wftcdujp9xnYjsD8130_provenance.