Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion description "[This rare disease is associated with loss of heterozygosity (LOH) on chromosome 11q13, the locus of the MEN-1 gene, although the MEN-1 sequence and expression appear normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion evidence source_evidence_literature NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion SIO_000772 10690880 NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion wasDerivedFrom befree-20140225 NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion wasGeneratedBy ECO_0000203 NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_provenance.