Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_assertion description "[These findings confirm that germline GATA2 mutations predispose to familial myelodysplastic syndrome/acute myeloid leukemia, and that monosomy 7 and ASXL1 mutations may be recurrent secondary genetic abnormalities triggering overt malignancy in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_assertion evidence source_evidence_literature NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_assertion SIO_000772 22271902 NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_assertion wasDerivedFrom befree-20140225 NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_assertion wasGeneratedBy ECO_0000203 NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP602049.RAG9GF2z2Cs6unzX3qocrL2_PzpE5ShRy62ACKXZ1Ad9Y130_provenance.