Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_assertion description "[We found that gtdc2 knockdown in zebrafish replicates all WWS features (hydrocephalus, ocular defects, and muscular dystrophy), strongly suggesting that GTDC2 mutations cause WWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_assertion evidence source_evidence_literature NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_assertion SIO_000772 22958903 NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_assertion wasDerivedFrom befree-20150227 NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_assertion wasGeneratedBy ECO_0000203 NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.
- befree-20150227 importedOn "2015-02-27" NP958501.RAcEor35_CXa-Rx8sJ8bluaFj1mc_R4_ADHlbxXIc7Hok130_provenance.