Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_assertion description "[We conclude that the 5q-syndrome may be best defined as primary MDS of the FAB type RA with a 5q deletion as the sole karyotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_assertion evidence source_evidence_literature NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_assertion SIO_000772 7604812 NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_assertion wasDerivedFrom befree-20150227 NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_assertion wasGeneratedBy ECO_0000203 NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP913883.RA01ai7tIMZx4s4YA2tkODqdVnlQ02pCYzvbauAXYjMIA130_provenance.