Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_assertion description "[This showed that the two nuclear envelope defects (EDMD LMNA, EDMD emerin) were highly related disorders and were also related to fascioscapulohumeral muscular dystrophy (FSHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_assertion evidence source_evidence_literature NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_assertion SIO_000772 16478798 NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_assertion wasDerivedFrom befree-20140225 NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_assertion wasGeneratedBy ECO_0000203 NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276530.RAZ8yJxccb_E5oDrn_9RQpuKuWn2aSRmerYQhZjZc5i6U130_provenance.