Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_assertion description "[Subsequent fluorescence in-situ hybridization and Array-CGH analyses revealed an unbalanced translocation between 9p and 15q resulting in a partial monosomy of 9p and a partial trisomy of 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_assertion evidence source_evidence_literature NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_assertion SIO_000772 20671549 NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_assertion wasDerivedFrom befree-2016 NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_assertion wasGeneratedBy ECO_0000203 NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP829593.RAbt-PZtJ1x6I4fXMQu51eINphTLGUKp5EbD4i7nQb61Y130_provenance.