Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_assertion> ?p ?o ?g. }
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- NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_assertion type Assertion NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_head.
- NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_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." NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_provenance.
- NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_assertion evidence source_evidence_literature NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_provenance.
- NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_assertion SIO_000772 8931691 NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_provenance.
- NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_assertion wasDerivedFrom befree-2016 NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_provenance.
- NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_assertion wasGeneratedBy ECO_0000203 NP1362956.RALeCA5BL9cxmx2tsFCvr8qDn6x68Bg5v896HBuJS-EQo130_provenance.