Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_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." NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_assertion evidence source_evidence_literature NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_assertion SIO_000772 12921235 NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_assertion wasDerivedFrom befree-2016 NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_assertion wasGeneratedBy ECO_0000203 NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.
- befree-2016 importedOn "2016-02-19" NP405753.RARYDdlFEu18XHGCB7YdgVuXEK35pGu3dib-dO4auixpU130_provenance.