Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_assertion wasGeneratedBy ECO_0000203 NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_assertion wasDerivedFrom befree-20150227 NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_assertion SIO_000772 9604756 NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_assertion evidence source_evidence_literature NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.
- NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_assertion description "[The application of simultaneous amplification of the above linked polymorphic markers allowed detection of more than half of the cases of ADO in blastomeres (19.4% for cystic fibrosis and 12.3% for beta-globin gene) and almost all ADOs in polar bodies, particularly when the two-step sequential analysis of the first and second polar body was applied in preimplantation diagnosis of single gene disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444272.RAV2AWH_1H5sD9moXBUXeEip0UZ2GDgXakW9HvQ3r5bmY130_provenance.