Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion> ?p ?o ?g. }
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- NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion type Assertion NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_head.
- NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion description "[We first screened 153 patients with MR and facial dysmorphism associated with malformations, or growth anomalies, or familial history, with cytogenetically normal chromosomes, and the absence of FRAXA mutation and subtelomeric rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_provenance.
- NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion evidence source_evidence_literature NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_provenance.
- NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion SIO_000772 16773131 NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_provenance.
- NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion wasDerivedFrom befree-20150227 NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_provenance.
- NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_assertion wasGeneratedBy ECO_0000203 NP408919.RAIUes9mjN_nLHvZPeTDYIrggPEc5zZQQZ5pMEDTLwf0I130_provenance.