Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_assertion description "[Among the most sensitive were lines with rearrangements of CRLF2, which is overexpressed in ~ 10% of B-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_assertion evidence source_evidence_literature NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_assertion SIO_000772 22904298 NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_assertion wasDerivedFrom befree-20140225 NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_assertion wasGeneratedBy ECO_0000203 NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.
- befree-20140225 importedOn "2014-02-25" NP274479.RAFOvya1LMttkIDusLMh8DPGlvlNHCIH7RT0GMNYVz718130_provenance.