Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion> ?p ?o ?g. }
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- NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion type Assertion NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_head.
- NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion wasGeneratedBy ECO_0000203 NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_provenance.
- NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion wasDerivedFrom befree-2016 NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_provenance.
- NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion SIO_000772 16987873 NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_provenance.
- NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion evidence source_evidence_literature NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_provenance.
- NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_assertion description "[The finding of a significant number of copy number polymorphisms in the genome in the normal population, means that assigning pathogenicity to deletions and duplications in patients with mental retardation can be difficult but has been identified for duplications of MECP2 and L1CAM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570297.RArlC-y_NPgDPHNpC1CKEYZqdZWAvsQ2Ui2uFnW_2y9MY130_provenance.