Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion> ?p ?o ?g. }
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- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion type Assertion NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_head.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion description "[Among the prognostically important aberrations, the del13q14 was present in 36 (51.4%), trisomy 12 in 9 (12.8%), del11q22 in 9 (12.8%), and del17p13 in 4 cases (5.7%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion evidence source_evidence_literature NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion SIO_000772 17053054 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion wasDerivedFrom befree-20150227 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion wasGeneratedBy ECO_0000203 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.