Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion type Assertion NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_head.
- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion wasGeneratedBy ECO_0000203 NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_provenance.
- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion wasDerivedFrom befree-20140225 NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_provenance.
- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion SIO_000772 21336781 NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_provenance.
- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion evidence source_evidence_literature NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_provenance.
- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_provenance.