Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_assertion description "[Myotonic dystrophy type 2 (DM2) is caused by CCTG-repeat expansions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_assertion evidence source_evidence_literature NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_assertion SIO_000772 23097607 NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_assertion wasDerivedFrom befree-20150227 NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_assertion wasGeneratedBy ECO_0000203 NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP758087.RApXIWsA1eGA8fVgGiHVs1CgK8J1Gsi5jdVIVjDOaT72Q130_provenance.