Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_assertion description "[However, 95% of CML patients have the ABL gene from chromosome 9 fused with the breakpoint cluster (BCR) gene from chromosome 22, resulting in a short chromosome known as the Philadelphia chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_assertion evidence source_evidence_curated NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_assertion SIO_000772 18673174 NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_assertion wasDerivedFrom ctd_human-20150221 NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_assertion wasGeneratedBy ECO_0000218 NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP8253.RArirFDhSvPcwCdUHuupvSilY-3mci0q_zgCmFGEl2_8g130_provenance.