Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_assertion description "[Mutations in the lamin A/C gene determine a heterogeneous group of congenital diseases, termed laminopathies, consisting of more than 15 phenotypes, including autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_assertion evidence source_evidence_literature NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_assertion SIO_000772 20837309 NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_assertion wasDerivedFrom befree-20150227 NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_assertion wasGeneratedBy ECO_0000203 NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537627.RAhmrqTl5sYr0m_pUDzyn0Vd4xNtA82UpC9DzZUc2Wnms130_provenance.