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- NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_assertion type Assertion NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_head.
- NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_assertion wasGeneratedBy ECO_0000203 NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_provenance.
- NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_assertion wasDerivedFrom befree-20150227 NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_provenance.
- NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_assertion SIO_000772 16987873 NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_provenance.
- NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_assertion evidence source_evidence_literature NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_provenance.
- NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_assertion description "[Novel autosomal genes that cause mental retardation have been identified recently including CC2D1A identified by homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914962.RAkYOouvel0UMOK5pUIwu2NL3AzJzkyXjaHwM-Hdf5_Ro130_provenance.