Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_assertion description "[The cytogenetic anomaly der(20)del(20)(q11.2q13.3)idic(20)(p11), or idic(20q-) in short form, has been reported in 13 cases of myelodysplastic syndrome, one case of chronic myelomonocytic leukemia, and one case of acute myeloid leukemia since 2004.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_assertion evidence source_evidence_literature NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_assertion SIO_000772 18262055 NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_assertion wasDerivedFrom befree-20140225 NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_assertion wasGeneratedBy ECO_0000203 NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP233599.RAuiNAQ1TTLuRT2iZZNRF_9A2UI3wwkPrYLgM103G1FOM130_provenance.