Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_assertion description "[Her 2-year-old son with Duchenne muscular dystrophy (DMD)_had no demonstrable deletion in the dystrophin gene, but all fibers except for 5% 'revertant' fibers in a muscle biopsy specimen had no dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_assertion evidence source_evidence_literature NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_assertion SIO_000772 7573761 NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_assertion wasDerivedFrom befree-2016 NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_assertion wasGeneratedBy ECO_0000203 NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313052.RAWVVy84eQc7JRuHgXBgaVe9oraUgkxYHeRL6AwyIROhs130_provenance.