Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_assertion description "[An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_assertion evidence source_evidence_literature NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_assertion SIO_000772 1558976 NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_assertion wasDerivedFrom gad-20150221 NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_assertion wasGeneratedBy ECO_0000203 NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP89427.RAkrl4QhZZj1fqf15w3O0jGEUtwHhxF7F6Oib3QuS4yNY130_provenance.