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- NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_assertion type Assertion NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_head.
- NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_assertion description "[The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_provenance.
- NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_assertion evidence source_evidence_literature NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_provenance.
- NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_assertion SIO_000772 16033914 NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_provenance.
- NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_assertion wasDerivedFrom befree-2016 NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_provenance.
- NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_assertion wasGeneratedBy ECO_0000203 NP505130.RAeHzbwF-ufusTnqrow-gr4Ti7FSX9hveOZfTyO7zn_hk130_provenance.