Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_assertion description "[There was a very strong correlation of clinical diagnoses with the type of dystrophin abnormality; all Duchenne muscular dystrophy patient muscle contained no detectable dystrophin, Becker muscular dystrophy patient muscle had clearly abnormal dystrophin, and unrelated diseases showed normal dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_assertion evidence source_evidence_literature NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_assertion SIO_000772 2674948 NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_assertion wasDerivedFrom befree-2016 NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_assertion wasGeneratedBy ECO_0000203 NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295908.RAgUz0ykuQ-IQdxfkQgjcQiSGGPn2GBPJVWFtHF6w2k5g130_provenance.