Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_assertion description "[Here we report the experience of our group in the counselling and molecular prenatal diagnosis of three inherited neuromuscular diseases, i.e., Duchenne/Becker muscular dystrophy (DMD/BMD), myotonic dystrophy type 1 (DM1), spinal muscular atrophy (SMA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_assertion evidence source_evidence_literature NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_assertion SIO_000772 23729582 NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_assertion wasDerivedFrom befree-2016 NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_assertion wasGeneratedBy ECO_0000203 NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.
- befree-2016 importedOn "2016-02-19" NP1082884.RA1TW7LmESac0Kzik1MPrx2WRhcGaRJTASSxEFg7Qgi04130_provenance.