Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion> ?p ?o ?g. }
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- NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion type Assertion NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_head.
- NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion description "[This study reports 12 novel mutations of the Wilson disease (WD) gene which have been detected by the molecular analysis of 29 patients of Mediterranean descent carrying uncommon chromosomal haplotypes at the WD locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_provenance.
- NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion evidence source_evidence_literature NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_provenance.
- NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion SIO_000772 8931691 NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_provenance.
- NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion wasDerivedFrom befree-2016 NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_provenance.
- NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_assertion wasGeneratedBy ECO_0000203 NP1362955.RABcr0ygaNx8U_rW_WjatIQme1Vhq0GsRrOftuTgnm0SI130_provenance.