Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_assertion description "[The detection rate of chromosomal abnormalities by four different approaches were compared: (i) karyotyping for all samples; (ii) RAD (21,18,13,X,Y) for all samples; (iii) RAD for all samples + karyotyping for cases with ultrasound abnormalities; and (iv) RAD (21,18,13) for all + RAD (X,Y) for cases with ultrasound abnormalities consistent with Turner syndrome + karyotyping for cases with ultrasound abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_assertion evidence source_evidence_literature NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_assertion SIO_000772 16421217 NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_assertion wasDerivedFrom befree-20140225 NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_assertion wasGeneratedBy ECO_0000203 NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP920833.RAK-p2z9GbkbF53Y1TX50LffJbVuqWgDs4hF8A5nqp9NY130_provenance.