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- source_evidence_literature type ECO_0000212 NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_assertion description "[Sequence analysis of the tumor suppressor gene ASXL1, which is located in 20q and is commonly mutated in malignant myeloid diseases and occasionally in CLL/SLL specimens, revealed no mutations in our three patients with copy neutral LOH in 20q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_assertion evidence source_evidence_literature NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_assertion SIO_000772 24704113 NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_assertion wasDerivedFrom befree-20150227 NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_assertion wasGeneratedBy ECO_0000203 NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978468.RAfj2VIkNd6_Mjalt51Nldg7tUz9vahDOqWnCzx9gjBLM130_provenance.