Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion> ?p ?o ?g. }
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- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion type Assertion NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_head.
- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_provenance.
- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion evidence source_evidence_literature NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_provenance.
- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion SIO_000772 23615299 NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_provenance.
- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion wasDerivedFrom befree-20140225 NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_provenance.
- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion wasGeneratedBy ECO_0000203 NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_provenance.