Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_assertion description "[Negative results for transmission disequilibrium of polymorphisms of HTR2C and MAOA with autism were provided from German and Austrian families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_assertion evidence source_evidence_literature NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_assertion SIO_000772 10374746 NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_assertion wasDerivedFrom befree-20150227 NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_assertion wasGeneratedBy ECO_0000203 NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP471758.RATOetlnR-FdyDxuQntzgmlE7L2DQlX6y5VgYhm-A37d4130_provenance.