Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion> ?p ?o ?g. }
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- NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_assertion type Assertion NP569081.RA9T4XZhDuWVzdByhjSP22bLWEllkFphBeaDwM1VZ3NxQ130_head.
- 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.