Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_assertion description "[Acute myeloid leukemia with myelodysplasia-related changes are characterized by a specific molecular pattern with high frequency of ASXL1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_assertion evidence source_evidence_literature NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_assertion SIO_000772 22535592 NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_assertion wasDerivedFrom befree-20140225 NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_assertion wasGeneratedBy ECO_0000203 NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP278811.RAHyV6-9aESNS-9O8Is14lxO_2KBLcvYl3_OKvvmMrhVc130_provenance.