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- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion type Assertion NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_head.
- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_provenance.
- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion evidence source_evidence_literature NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_provenance.
- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion SIO_000772 8830776 NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_provenance.
- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion wasDerivedFrom befree-20140225 NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_provenance.
- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion wasGeneratedBy ECO_0000203 NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_provenance.