Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_assertion description "[We screened the FOXG1 gene in a cohort of 206 MECP2 and CDKL5 mutation negative patients (136 females and 70 males) with severe encephalopathy and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_assertion evidence source_evidence_literature NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_assertion SIO_000772 19806373 NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_assertion wasDerivedFrom befree-20140225 NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_assertion wasGeneratedBy ECO_0000203 NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP235348.RASXF887bR4nGIAuQVF85Mph1Wkji9UubwEaEpEPMW8Gk130_provenance.