Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_assertion description "[The phenotype HP1 was found to have an increased incidence in the total patient group due to an increased incidence in those with AML, ALL and CML compared with controls, but not in those with CLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_assertion evidence source_evidence_literature NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_assertion SIO_000772 3397067 NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_assertion wasDerivedFrom befree-20140225 NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_assertion wasGeneratedBy ECO_0000203 NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651016.RAzyDO5tDC3Q7AAhkjg72yNYcmA1RIfHKNvYfb9kQz3Y8130_provenance.