Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_assertion description "[The results of our study suggest that mutations in HNF3B are not a common cause of MODY in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_assertion evidence source_evidence_literature NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_assertion SIO_000772 10868948 NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_assertion wasDerivedFrom gad-20150221 NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_assertion wasGeneratedBy ECO_0000203 NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67803.RArbnXGzwP9usrt7oOqLJforzjSc2Hd3jkw0PGQkDyUQ0130_provenance.