Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_assertion description "[Although hst gene rearrangements and deletions of 11q13 are not associated with sporadic PRL-cell adenoma formation, a single patient was detected with a partial loss of chromosome 11, including the putative MEN-1 site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_assertion evidence source_evidence_literature NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_assertion SIO_000772 8100831 NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_assertion wasDerivedFrom befree-20150227 NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_assertion wasGeneratedBy ECO_0000203 NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720267.RABPCkWMt_LLKlhXfrr0Q_ncyltxqKS9VkmCaecXfdNtY130_provenance.