Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion> ?p ?o ?g. }
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- NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion type Assertion NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_head.
- NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion description "[We conclude that EFMR is a distinctive, under-recognized familial syndrome where girls present with convulsions in infancy, often associated with intellectual impairment and autistic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_provenance.
- NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion evidence source_evidence_literature NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_provenance.
- NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion SIO_000772 18234694 NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_provenance.
- NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion wasDerivedFrom befree-20140225 NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_provenance.
- NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_assertion wasGeneratedBy ECO_0000203 NP937121.RASLq3BT5nMEkfsw0OA75V2pDkGerDrGyZsPCwbqvks_g130_provenance.