Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_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." NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_assertion evidence source_evidence_literature NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_assertion SIO_000772 18646565 NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_assertion wasDerivedFrom befree-2016 NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_assertion wasGeneratedBy ECO_0000203 NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.
- befree-2016 importedOn "2016-02-19" NP683778.RA3wz4VIDXQwhlgZpf1KL11_idvCW_N-K1SGkwDgFT5fU130_provenance.