Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_assertion description "[Morphological, clinical and cytogenetic assessment revealed the typical hallmarks of 3q26/EVI1 rearrangements, that is, trilineage dysplasia and dysmegakaryopoiesis, poor prognosis and additional monosomy 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_assertion evidence source_evidence_literature NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_assertion SIO_000772 15085164 NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_assertion wasDerivedFrom befree-2016 NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_assertion wasGeneratedBy ECO_0000203 NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.
- befree-2016 importedOn "2016-02-19" NP440011.RAOP76aoTNbUOSqltXTdttoqsTBLmtv2COdyaH1TtsUmE130_provenance.