Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion> ?p ?o ?g. }
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- NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion type Assertion NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_head.
- NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion description "[Therefore, this case suggests that a new gene may be associated with congenital muscular dystrophy with alpha-dystroglycan glycosylation defects, cortical migration defects, and sparing of the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_provenance.
- NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion evidence source_evidence_literature NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_provenance.
- NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion SIO_000772 19633331 NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_provenance.
- NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion wasDerivedFrom befree-2016 NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_provenance.
- NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_assertion wasGeneratedBy ECO_0000203 NP753532.RAB4OsFypWmuJfGTsIwpJKNkvX58nRRBnp_2hXtoQVEr8130_provenance.