Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_assertion> ?p ?o ?g. }
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- NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_assertion type Assertion NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_head.
- NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_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." NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_provenance.
- NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_assertion evidence source_evidence_literature NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_provenance.
- NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_assertion SIO_000772 16773131 NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_provenance.
- NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_assertion wasDerivedFrom befree-20150227 NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_provenance.
- NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_assertion wasGeneratedBy ECO_0000203 NP412592.RAtYBSBQ44lI58rWABkEjsWFRu0mcUrPNodJ4kA1We9ww130_provenance.