Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_assertion wasGeneratedBy ECO_0000203 NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_assertion wasDerivedFrom gad-20130706 NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_assertion SIO_000772 18685874 NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_assertion evidence source_evidence_literature NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_assertion description "[The location of DCX mutations predicts malformation severity in X-linked lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP76141.RAN1NZKv_YNXs2F4Btmlhe2m2NuLjFo7q-Ggpa9OfSrGA130_provenance.