Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_assertion description "[We discuss the possible roles of a position effect or haploinsufficiency of distally located genes (e.g., CRKL) in the molecular pathogenesis of the 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_assertion evidence source_evidence_literature NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_assertion SIO_000772 22893440 NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_assertion wasDerivedFrom befree-20140225 NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_assertion wasGeneratedBy ECO_0000203 NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP405561.RAFHCLMTf1oIVwwIxs0wFFFYNmBFag2FZe3EFawgvf-hk130_provenance.