Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- befree-2016 importedOn "2016-02-19" NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion wasGeneratedBy ECO_0000203 NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion wasDerivedFrom befree-2016 NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion SIO_000772 10818214 NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion evidence source_evidence_literature NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.
- NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion description "[We have recently shown that mutations in oligophrenin-1 (OPHN1) are responsible for non-specific X-linked mental retardation (MRX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_provenance.