http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016207325-A1

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filingDate 2016-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2016-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2016207325-A1
titleOfInvention Method for detecting chromosomal abnormalities
abstract The invention relates to a method for identifying chromosomal abnormalities, particularly structural and/or numerical chromosomal abnormalities, and preferably structural chromosomal abnormalities, using in-situ hybridisation by detecting chromosomes and/or DNA regions in a biological sample, preferably in one or more cell(s) and/or in one or more cell nuclei.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4911
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1958
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3847

Total number of triples: 651.