Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion> ?p ?o ?g. }
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- NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion type Assertion NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_head.
- NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion description "[The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_provenance.
- NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion evidence source_evidence_literature NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_provenance.
- NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion SIO_000772 20591486 NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_provenance.
- NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion wasDerivedFrom befree-20140225 NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_provenance.
- NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_assertion wasGeneratedBy ECO_0000203 NP320388.RAwN6ZtUY1BX0TWOO1LrZzYtQAbTUDwUlwPVYP8VI1bPQ130_provenance.