Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_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." NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_assertion evidence source_evidence_literature NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_assertion SIO_000772 17560787 NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_assertion wasDerivedFrom lhgdn-20090331 NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_assertion wasGeneratedBy ECO_0000203 NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP226101.RADKPY8On5K8eTzLPJC4AJaPXMGgBIFqAkPl20uZv26og130_provenance.