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- source_evidence_literature type ECO_0000212 NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_assertion description "[Hypomorphic mutations in the NBS1 and MRE11 genes lead to two other genomic instability disorders: the Nijmegen breakage syndrome (NBS) and A-T like disease (A-TLD), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_assertion evidence source_evidence_literature NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_assertion SIO_000772 14532133 NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_assertion wasDerivedFrom befree-20150227 NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_assertion wasGeneratedBy ECO_0000203 NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568900.RAsgfM0F7LmBJAYY6uDiDKcf0ylJ0KF0eyF-NhvUKrzpg130_provenance.