Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_assertion wasGeneratedBy ECO_0000203 NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_assertion wasDerivedFrom befree-20140225 NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_assertion SIO_000772 9748047 NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_assertion evidence source_evidence_literature NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876790.RACreHwqm7M9buJSzFcAH1oMNLJOFAMJjrzFul_AzVAek130_provenance.