Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion> ?p ?o ?g. }
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- NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion type Assertion NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_head.
- NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion wasGeneratedBy ECO_0000203 NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance.
- NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion wasDerivedFrom befree-20140225 NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance.
- NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion SIO_000772 18694825 NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance.
- NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion evidence source_evidence_literature NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance.
- NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion description "[In severe ID, cytogenetically visible chromosomal abnormalities like trisomy 21 continue to be common, but since the introduction of array CGH, it is becoming clear that submicroscopic deletions and duplications are equally frequent, yet previously overlooked causes of ID.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance.