Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion> ?p ?o ?g. }
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- NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion type Assertion NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_head.
- NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion description "[We pooled clinical data of all published carriers of lamin A/C gene mutations as cause of skeletal and/or cardiac muscle disease and reviewed ECG findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_provenance.
- NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion evidence source_evidence_literature NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_provenance.
- NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion SIO_000772 15551023 NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_provenance.
- NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion wasDerivedFrom befree-2016 NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_provenance.
- NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_assertion wasGeneratedBy ECO_0000203 NP469576.RAX3exROZIdvDAC7Lt8V2dtlKjWlIQ5yeL4wsr1uW6P3U130_provenance.