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- source_evidence_literature type ECO_0000212 NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP215439.RANIxs1AjTCf67g_hNiNaU6mhW9Ev43P0aEd9yilZlfRk130_provenance.