摘要:
A method for simplifying an extensible markup language (XML) schema, including: identifying data in an instance specification as variable or fixed, wherein the instance specification corresponds to a complex XML schema; determining a set of types including the variable data, wherein the set of types conforms to a structure of the complex XML schema; capturing the set of types as metadata annotations associated with the instance specification; and generating a simplified XML schema from the instance specification, wherein the simplified XML schema is stored on a memory device.
摘要:
Novel splice variant nucleic acid sequences. The novel splice variants and their nucleic acid sequences according to the present invention may optionally be used for diagnosis of a variant-detectable disease as described herein.
摘要:
A method and system for querying a Health Level 7 (HL7) data repository which stores entries in HL7 Reference Information Model (RIM) terminology across multiple HL7 domains. The method includes: receiving a query input to retrieve data from the repository, wherein the query input is in a query language, converting the query input to a RIM query, and retrieving data from the repository using the RIM query. The RIM query expresses the query input using RIM physical classes and RIM codes. The method also includes converting retrieved RIM instances from the repository to a domain readable format. Providing the data repository includes receiving data for input in the data repository, wherein the data for input is defined at a domain level as a domain instance, and converting a domain instance to a RIM instance and inputting the RIM instance in the data repository.
摘要:
Novel splice variant nucleic acid sequences. The novel splice variants and their nucleic acid sequences according to the present invention may optionally be used for diagnosis of a variant-detectable disease as described herein.