Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_assertion description "[Autosomal dominant gain-of-function truncations of CXCR4 are associated with warts, hypo-gammaglobulinemia, infections, and myelokathexis (WHIM) syndrome, a primary immunodeficiency disorder characterized by neutropenia and recurrent infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_assertion evidence source_evidence_literature NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_assertion SIO_000772 20592249 NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_assertion wasDerivedFrom befree-20150227 NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_assertion wasGeneratedBy ECO_0000203 NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784971.RA4WmEKyF4ImRVS6sJwZsQ_9kQVjCVVd0X1o6REPI4PPc130_provenance.