Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion> ?p ?o ?g. }
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- NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion type Assertion NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_head.
- NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion description "[Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_provenance.
- NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion evidence source_evidence_curated NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_provenance.
- NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion SIO_000772 20729831 NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_provenance.
- NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion wasDerivedFrom uniprot-20130724 NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_provenance.
- NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_assertion wasGeneratedBy ECO_0000218 NP7068.RACMGkW6lmLgR4nyo5obPdCQ5q5vxfdV_Z2EA69p0CACE130_provenance.