Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_assertion description "[We investigated the occurrence of mutations in the G-CSF receptor in eight patients with AA who developed MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_assertion evidence source_evidence_literature NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_assertion SIO_000772 11122117 NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_assertion wasDerivedFrom befree-20140225 NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_assertion wasGeneratedBy ECO_0000203 NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723054.RABkhW5D6eJmwZBjd-Br3Ln05qM84ME6kiPDoekCl-lRk130_provenance.