Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion description "[Mutations of the lamin A/C gene are associated with several different neuromuscular diseases, and the detailed effect of disease-associated amino acid substitutions on the structure and stability of human lamin dimers is yet unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion evidence source_evidence_literature NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion SIO_000772 23142632 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion wasDerivedFrom befree-20150227 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion wasGeneratedBy ECO_0000203 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.