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- source_evidence_literature type ECO_0000212 NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_assertion description "[Given the observed clinical variability of Becker dystrophy, it appears that dystrophin analysis is required for accurately distinguishing between Becker dystrophy and clinically similar autosomal recessive myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_assertion evidence source_evidence_literature NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_assertion SIO_000772 2668783 NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_assertion wasDerivedFrom befree-2016 NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_assertion wasGeneratedBy ECO_0000203 NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295807.RAXEfmtDqRiHMNTvRcY3GChh2uSAhAGbwH31k44-bxcqQ130_provenance.