Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_assertion description "[We analyzed the role of the three known CACNA1S gene mutations (R528H, R1239H, and R1239G) in Chinese patients, including two FPP families, 36 TPP patients, 12 SPP patients, and their relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_assertion evidence source_evidence_literature NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_assertion SIO_000772 15711422 NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_assertion wasDerivedFrom gad-20150221 NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_assertion wasGeneratedBy ECO_0000203 NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90638.RAY_HWE3XD3AL9OKfEfHnFvYaSKNnN4rV0qwqvrguQeLU130_provenance.