Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_assertion description "[Two mutated HEXA alleles in a Druze patient with late-infantile Tay-Sachs disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_assertion evidence source_evidence_curated NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_assertion SIO_000772 9401008 NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_assertion wasDerivedFrom uniprot-20150221 NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_assertion wasGeneratedBy ECO_0000218 NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1184.RATlXkFFEbR6Crs119UPzIk3H5ssgF4q4GI0BX747uHjo130_provenance.