Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_assertion description "[For instance, a point mutation in a human clock gene (Per2) was shown to produce the rare advanced sleep phase syndrome, whereas a functional polymorphism in Per3 is associated with the more frequent delayed sleep phase syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_assertion evidence source_evidence_literature NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_assertion SIO_000772 16979429 NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_assertion wasDerivedFrom befree-2016 NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_assertion wasGeneratedBy ECO_0000203 NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.
- befree-2016 importedOn "2016-02-19" NP569610.RApgYk0gVhbh15TEwZ3dwMcYKsShSijxbn7ena5n7bVtE130_provenance.