Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_assertion description "[OCA2 (MIM 203200), the most common form of OCA, is associated with mutations of the P gene and accounts for approximately 50% of OCA worldwide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_assertion evidence source_evidence_literature NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_assertion SIO_000772 11574907 NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_assertion wasDerivedFrom befree-2016 NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_assertion wasGeneratedBy ECO_0000203 NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.
- befree-2016 importedOn "2016-02-19" NP331297.RAY1tNgliSs7vD7XeORWAr12QX7nXRVe4A1mDyncFwZB4130_provenance.