Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_assertion description "[Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_assertion evidence source_evidence_literature NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_assertion SIO_000772 18253031 NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_assertion wasDerivedFrom befree-2016 NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_assertion wasGeneratedBy ECO_0000203 NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.
- befree-2016 importedOn "2016-02-19" NP654029.RAXGq3lnV4i3CW0W3h3pHh54DtxVDDni3yrnQF4Jc2QRo130_provenance.