Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_assertion description "[The two known loci for X-linked mental retardation and spastic paraplegia are excluded: proteolipid protein in Xp21 and L1 cell adhesion molecule in Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_assertion evidence source_evidence_literature NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_assertion SIO_000772 10982473 NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_assertion wasDerivedFrom befree-2016 NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_assertion wasGeneratedBy ECO_0000203 NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP294788.RAY4TtYXtVvlGrfp5H4gXGDP68tor5T47wQUkFAr0JJSQ130_provenance.