Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_assertion description "[However, mutations in two nuclear proteins--emerin and lamin A/C--have also been demonstrated to give rise to a muscular dystrophy phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_assertion evidence source_evidence_literature NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_assertion SIO_000772 14585157 NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_assertion wasDerivedFrom befree-2016 NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_assertion wasGeneratedBy ECO_0000203 NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.
- befree-2016 importedOn "2016-02-19" NP418676.RAVVRFRGFEP3T5L6fJoyXiOTnacgNXfBDyMk4N3ypKJnI130_provenance.