Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_assertion> ?p ?o ?g. }
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- NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_assertion type Assertion NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_head.
- NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_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." NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_provenance.
- NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_assertion evidence source_evidence_literature NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_provenance.
- NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_assertion SIO_000772 10690880 NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_provenance.
- NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_assertion wasDerivedFrom befree-20150227 NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_provenance.
- NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_assertion wasGeneratedBy ECO_0000203 NP553623.RAo4mi7reArI56o264CJulKpmTBOyU1ZFG3twnNOMqGVg130_provenance.