Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion> ?p ?o ?g. }
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- NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion type Assertion NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_head.
- NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion description "[In women with McArdle's disease, ACTN3 genotypes might partly explain the large individual variability that exists in the phenotypic manifestation of this disorder]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion evidence source_evidence_literature NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion SIO_000772 17560787 NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion wasDerivedFrom lhgdn-20090331 NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_assertion wasGeneratedBy ECO_0000203 NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.