Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_assertion description "[WHIM is an acronym for a rare immunodeficiency syndrome (OMIM #193670) caused by autosomal dominant mutations truncating the C-terminus of the chemokine receptor CXC chemokine receptor 4 (CXCR4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_assertion evidence source_evidence_literature NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_assertion SIO_000772 21070597 NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_assertion wasDerivedFrom befree-20150227 NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_assertion wasGeneratedBy ECO_0000203 NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.