Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_assertion description "[These human congenital muscular dystrophies and the myd mouse are associated with defective glycosylation of alpha-dystroglycan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_assertion evidence source_evidence_literature NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_assertion SIO_000772 15229394 NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_assertion wasDerivedFrom befree-2016 NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_assertion wasGeneratedBy ECO_0000203 NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.
- befree-2016 importedOn "2016-02-19" NP450480.RAXhDtZSXEKA0T3MC0-lYv0-VRZF02laH-Sb8_O4AC-Fg130_provenance.