Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_assertion description "[By using multiple polymerase reaction (mPCR) and haploid analysis of 11 short tandem repeats (STRs) in dystrophin gene locus to identify female carriers in deletional DMD/BMD (Duchenne/Becker Muscular Dystrophy) families, valuable information can be gathered for prenatal diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_assertion evidence source_evidence_literature NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_assertion SIO_000772 16553208 NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_assertion wasDerivedFrom befree-2016 NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_assertion wasGeneratedBy ECO_0000203 NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.
- befree-2016 importedOn "2016-02-19" NP541550.RAQNhziYmh3ItwtNMI2YbMZsYiOxIj3F-BIHKYOOKNVYw130_provenance.