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- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion type Assertion NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_head.
- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_provenance.
- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion evidence source_evidence_literature NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_provenance.
- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion SIO_000772 11941538 NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_provenance.
- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion wasDerivedFrom lhgdn-20090331 NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_provenance.
- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion wasGeneratedBy ECO_0000203 NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_provenance.