Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_assertion wasGeneratedBy ECO_0000203 NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_assertion wasDerivedFrom befree-20140225 NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_assertion SIO_000772 19417767 NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_assertion evidence source_evidence_literature NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.