Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_assertion evidence source_evidence_literature NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_assertion SIO_000772 17635637 NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_assertion wasDerivedFrom befree-2016 NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_assertion wasGeneratedBy ECO_0000203 NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.