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- source_evidence_literature type ECO_0000212 NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion description "[Somatic cell testing of dystrophin expression may offer an alternative to established genetic carrier tests for those women in whom deletions of the DMD are not detectable, whose pedigree structure does not permit linkage analysis, or in whom standard phenotypic analyses are ambiguous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion evidence source_evidence_literature NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion SIO_000772 2658563 NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion wasDerivedFrom befree-2016 NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion wasGeneratedBy ECO_0000203 NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance.