Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_assertion description "[Hence, these studies identify novel biological functions for merosin in myoblast fusion and muscle cell survival; furthermore, these explain some of the pathogenic events observed in congenital muscular dystrophy caused by merosin deficiency and provide in vitro models to further investigate the molecular mechanisms of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_assertion evidence source_evidence_literature NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_assertion SIO_000772 8830776 NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_assertion wasDerivedFrom befree-2016 NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_assertion wasGeneratedBy ECO_0000203 NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1358570.RAcFKHIUHSdmK0H90QDKgjSC95JwFTCvSin3wgShS6PJk130_provenance.