Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_assertion description "[To our knowledge, ARX mutation causing PMG and PVNH is unique, but the spasms and ACC are common in ARX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_assertion evidence source_evidence_literature NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_assertion SIO_000772 22585566 NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_assertion wasDerivedFrom befree-2016 NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_assertion wasGeneratedBy ECO_0000203 NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP982205.RANDqpJ0OX6Mo_FBhH46b8D9vK4C1dLtDMqw-453J8FsU130_provenance.