Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_assertion description "[The linkage region has been refined to a 24 cM region between D14S283 and D14S49 and mutations have been excluded in the PABP2 gene for oculopharyngeal muscular dystrophy which lies within this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_assertion evidence source_evidence_literature NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_assertion SIO_000772 12062252 NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_assertion wasDerivedFrom befree-2016 NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_assertion wasGeneratedBy ECO_0000203 NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.
- befree-2016 importedOn "2016-02-19" NP357652.RAhTKniCTqXolN12D29E0Iee8sO-nPgIp2-XYCAvdrh_4130_provenance.