Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_assertion description "[Recently, mutations in the CXCR4 chemokine receptor gene were identified in a dominantly inherited immunodeficiency disease, WHIM syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_assertion evidence source_evidence_literature NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_assertion SIO_000772 15661033 NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_assertion wasDerivedFrom befree-2016 NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_assertion wasGeneratedBy ECO_0000203 NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP477071.RATicCXB7bhf2Hr7jl5iiaKiYORJntayrXHEKJ6x_efNQ130_provenance.