Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_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." NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_assertion evidence source_evidence_literature NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_assertion SIO_000772 21727005 NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_assertion wasDerivedFrom befree-20140225 NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_assertion wasGeneratedBy ECO_0000203 NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212304.RAfTfvKZGgn07uUI-iEOH57-SW0ELchMTAewm3JGyLKng130_provenance.