Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_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." NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_assertion evidence source_evidence_literature NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_assertion SIO_000772 15661033 NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_assertion wasDerivedFrom befree-20150227 NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_assertion wasGeneratedBy ECO_0000203 NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784597.RAOqKC_-ESrtRlkLsav75f5ySBu25AdPAcIep1fe5cVQU130_provenance.