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- source_evidence_literature type ECO_0000212 NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_assertion description "[In analogy to symptomatic female dystrophinopathy carriers, our results suggest that heterozygous alpha-sarcoglycan gene mutation carriers can be symptomatic with selective muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_assertion evidence source_evidence_literature NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_assertion SIO_000772 14595658 NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_assertion wasDerivedFrom befree-20140225 NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_assertion wasGeneratedBy ECO_0000203 NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455477.RAsfDVLoKg-s7rXRsDQlH_ZzNQIL_1J06pHQ5hFNwyzEs130_provenance.