Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion> ?p ?o ?g. }
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- NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_assertion type Assertion NP284412.RAsYLh_DkYkajhaFxPKmrRkzRCq4o10RviDm-XnlwzW0s130_head.
- 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.