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- source_evidence_literature type ECO_0000212 NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_assertion description "[Five Duchenne muscular dystrophy -causing mutations in dystrophin gene, 697-698insGT, C616T, G1255T, C4279T, and C2302T, were identified in the new stop codons in downstream sites of mutations, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_assertion evidence source_evidence_literature NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_assertion SIO_000772 16883524 NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_assertion wasDerivedFrom lhgdn-20090331 NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_assertion wasGeneratedBy ECO_0000203 NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP207004.RA1126ikl-1FNd2CUy7LmWk01CtaE33uGY32b8DKyaxF8130_provenance.