Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_assertion description "[Together, the group of phenotypes associated with ARX mutations demonstrates remarkable pleiotropy, but also comprises a nearly continuous series of developmental disorders that begins with hydranencephaly, lissencephaly, and agenesis of the corpus callosum, and ends with a series of overlapping syndromes with apparently normal brain structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_assertion evidence source_evidence_literature NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_assertion SIO_000772 14722918 NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_assertion wasDerivedFrom befree-20140225 NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_assertion wasGeneratedBy ECO_0000203 NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921874.RA7iPx3_BpWH1dhO3aeVaZUfUgeqgg5XngDwlt7VpNGRQ130_provenance.