Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_assertion wasGeneratedBy ECO_0000203 NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_assertion wasDerivedFrom befree-2016 NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_assertion SIO_000772 23082473 NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_assertion evidence source_evidence_literature NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.
- NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_assertion description "[Chromosomal aberrations were found to be present in 76.6% of our patients with 13q deletion as the most frequent abnormality in our patients (46.7%), followed by trisomy 12 (36.7%), then ATM and p53 deletion (26.7%) each.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1022481.RAT1XYTxVpDQfr93Jha5WQqSm8aS18c7_Dveohoq1r6NU130_provenance.