Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- befree-2016 importedOn "2016-02-19" NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_assertion wasGeneratedBy ECO_0000203 NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_assertion wasDerivedFrom befree-2016 NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_assertion SIO_000772 15789066 NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_assertion evidence source_evidence_literature NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.
- NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_assertion description "[Although all patients displayed a BII/common phenotype, supernumerary Ph and trisomy 8 were associated with higher expression of CD19 and CD22 and of CD19, CD34, CD45, and HLA-DR, respectively; in turn, cases with monosomy 7 showed lower CD19, CD22, CD34, and cCD79a and del(9p21)(+) blasts were CD13(-) and CD33(-).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487110.RA6DqEji5T1akDni8a0ssYj0fP2aV0Oxo6NAdEzW4GXsw130_provenance.