Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_assertion description "[Analogous to the putative perturbation of the anchoring function of the dystrophin-associated complex in congenital muscular dystrophy with mutations in the alpha 2-subunit of laminin, our observations suggest a similar mechanism in Bethlem myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_assertion evidence source_evidence_literature NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_assertion SIO_000772 8782832 NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_assertion wasDerivedFrom befree-20150227 NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_assertion wasGeneratedBy ECO_0000203 NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355652.RAKDchghhymA487Mfdqi2yMEUJAl6Y9OknFhyNR1O0vrI130_provenance.