Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_assertion description "[Although ubiquitously expressed, DNM2 was found mutated in two genetic disorders affecting different tissues: autosomal dominant centronuclear myopathy (ADCNM; skeletal muscle) and peripheral Charcot-Marie-Tooth neuropathy (peripheral nerve).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_assertion evidence source_evidence_literature NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_assertion SIO_000772 21514436 NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_assertion wasDerivedFrom befree-20150227 NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_assertion wasGeneratedBy ECO_0000203 NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357013.RArPmbM2ePpbbTzAqgIIYoC0a2RUgeNhq1hYW7E0nf2Nk130_provenance.