Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion> ?p ?o ?g. }
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- NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion type Assertion NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_head.
- NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion wasGeneratedBy ECO_0000203 NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_provenance.
- NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion wasDerivedFrom befree-2016 NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_provenance.
- NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion SIO_000772 22739344 NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_provenance.
- NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion evidence source_evidence_literature NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_provenance.
- NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_assertion description "[We believe that the FOXG1 gene should be considered in severely mentally retarded patients (no speech-language) with severe acquired microcephaly (-4 to-6 SD) and few clinical features suggestive of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993583.RAKVwP9YfbMNg-bSXrPUmYgMm05YdQeQmaDTzVf35jPEw130_provenance.