Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_assertion description "[It is also estimated that 2.5-4% of male isolated patients diagnosed as DMD may have the AR form, which could be one possible explanation for the inconsistent results between clinical diagnosis and dystrophin assessment in one case recently reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_assertion evidence source_evidence_literature NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_assertion SIO_000772 2658592 NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_assertion wasDerivedFrom befree-2016 NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_assertion wasGeneratedBy ECO_0000203 NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295596.RAb5RIldV5FgXgDGx-V5SRRlYWWRrbIWEYI2KB7_nPtZw130_provenance.