Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_assertion description "[Mutations in the ARX gene, at Xp22.3, cause several disorders, including infantile spasms, X-linked lissencephaly with abnormal genitalia (XLAG), callosal agenesis and isolated intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_assertion evidence source_evidence_literature NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_assertion SIO_000772 22585566 NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_assertion wasDerivedFrom befree-20140225 NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_assertion wasGeneratedBy ECO_0000203 NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP566418.RAsvbL5Pt_w2rOdHAuyoSVNWiDJPBzDCBspBQLAvw9UcU130_provenance.