Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_assertion description "[Chromosomal breakpoints on chromosome 22 are located in the first intron of the bcr gene in half of the Philadelphia-positive acute leukemias (Ph1+bcr- AL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_assertion evidence source_evidence_literature NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_assertion SIO_000772 2648256 NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_assertion wasDerivedFrom befree-2016 NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_assertion wasGeneratedBy ECO_0000203 NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295083.RAPslxD-KWGm9r9137U1CZXu309XsjvSSxvWlHO48IQeU130_provenance.