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- source_evidence_literature type ECO_0000212 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion description "[We report two unrelated patients with MWS where the clinical diagnosis was established only after finding of disruption of the ZEB2 gene by a balanced translocation breakpoint and an interstitial microdeletion, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion evidence source_evidence_literature NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion SIO_000772 18445050 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion wasDerivedFrom befree-20150227 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion wasGeneratedBy ECO_0000203 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.