Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_assertion description "[To gain further information relating to the frequency, position and size of DNA deletions in the Duchenne/Becker muscular dystrophy (D/BMD) gene region, and to detect any correlation of these deletions with phenotype, a large clinic-based population of DMD and BMD patients has been investigated using 13 cloned intragenic sequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_assertion evidence source_evidence_literature NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_assertion SIO_000772 2653672 NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_assertion wasDerivedFrom befree-2016 NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_assertion wasGeneratedBy ECO_0000203 NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295408.RAUHD64CyMpOoBDzrdecpkdz0L3os6ne_RRsa_psFTvmk130_provenance.