Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_assertion description "[Mutations in the genes for nuclear envelope proteins of emerin (EMD) and lamin A/C (LMNA) are known to cause Emery-Dreifuss muscular dystrophy (EDMD) and limb girdle muscular dystrophy (LGMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_assertion evidence source_evidence_literature NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_assertion SIO_000772 18646565 NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_assertion wasDerivedFrom lhgdn-20090331 NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_assertion wasGeneratedBy ECO_0000203 NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP240281.RA2m0xxmDBBpfUKRkbZiDMbaNdhe8bZvkVkSioyBs9ZFI130_provenance.