Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_assertion description "[These diseases include Emery-Dreifuss muscular dystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy (DCM) with conduction system disease, familial partial lipodystrophy (FPLD), autosomal recessive axonal neuropathy (Charcot-Marie-Tooth disorder type 2, CMT2), mandibuloacral dysplasia (MAD), Hutchison Gilford Progeria syndrome (HGS), Greenberg Skeletal Dysplasia, and Pelger-Huet anomaly (PHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_assertion evidence source_evidence_literature NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_assertion SIO_000772 12921235 NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_assertion wasDerivedFrom befree-2016 NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_assertion wasGeneratedBy ECO_0000203 NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.
- befree-2016 importedOn "2016-02-19" NP405758.RALsc1-90vwKAvVI1iwINw4K8vm9F8_hI_N0B5Hnr9CHY130_provenance.