Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_assertion description "[ASXL1 haploinsufficiency is associated with a myelofibrosis phenotype in the context of other known and unknown lesions, and disruption of ASXL1 function may contribute to the disease pathogenesis of myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_assertion evidence source_evidence_literature NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_assertion SIO_000772 21712540 NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_assertion wasDerivedFrom befree-20140225 NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_assertion wasGeneratedBy ECO_0000203 NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP652977.RA6OHUDzHPGBl43wv_A4TOIj-PZ2SMDY-67YZXq6D3_tU130_provenance.