Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_assertion description "[These findings indicated that the frequency distribution of heterozygotes is not random within this population. Group C was further divided into C1, the 26 heterozygotes, and C2, the remaining 74 newborns in group C. In group C1 only 2 (8%) were in the 'h]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_assertion evidence source_evidence_literature NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_assertion SIO_000772 14970748 NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_assertion wasDerivedFrom gad-20150221 NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_assertion wasGeneratedBy ECO_0000203 NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76503.RALKnnfTMDw_pDLu4RKr6_GtSOk9wJqvFKJxcD1tKCzqU130_provenance.