Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_assertion description "[The most common histological variety was motor neurone disease type inclusion (MNDI) (n = 18), followed by corticobasal degeneration (CBD) (n = 12), then Pick's disease (n = 6), dementia lacking distinctive histology (DLDH) (n = 6) and PSP (n = 3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_assertion evidence source_evidence_literature NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_assertion SIO_000772 16033782 NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_assertion wasDerivedFrom befree-20140225 NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_assertion wasGeneratedBy ECO_0000203 NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273241.RAjzgSs45NNElcYxcjrIIuMsvQCh3wVWk6rqo8KfP51DU130_provenance.