Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_assertion description "[Other differences characterizing del(16q) included a lack of CNS relapses, lower incidences of eosinophilia and M4 FAB subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_assertion evidence source_evidence_literature NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_assertion SIO_000772 7596186 NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_assertion wasDerivedFrom befree-2016 NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_assertion wasGeneratedBy ECO_0000203 NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1314468.RAtzFuydLK_2b9FRCJ_9EnxWMYkzO565am3gdAVvciWLk130_provenance.