Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_assertion wasGeneratedBy ECO_0000203 NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_assertion wasDerivedFrom befree-20150227 NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_assertion SIO_000772 17650443 NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_assertion evidence source_evidence_literature NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.
- NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_assertion description "[Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285181.RAyVzir5FE-QEm_Mc1UvEf2h2MCAbjmVKh5_QL12o4phI130_provenance.