Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_assertion description "[The most severe phenotypes are Walker-Warburg Syndrome (WWS) and muscle-eye-brain disease (MEB) presenting with lissencephaly type II (LIS II) and in which muscular dystrophy is associated with mental retardation and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_assertion evidence source_evidence_literature NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_assertion SIO_000772 21727005 NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_assertion wasDerivedFrom befree-20140225 NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_assertion wasGeneratedBy ECO_0000203 NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614102.RA1qgu2_gG3_YqOv2z4zhvE-71NJwpWU7FpksMagS84eM130_provenance.