Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion> ?p ?o ?g. }
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- NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion type Assertion NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_head.
- NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion description "[PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_provenance.
- NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion evidence source_evidence_literature NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_provenance.
- NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion SIO_000772 18330912 NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_provenance.
- NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion wasDerivedFrom gad-20150221 NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_provenance.
- NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_assertion wasGeneratedBy ECO_0000203 NP120001.RAYsFXufoTig1M-0km0EVmo1Er58gGmPDTUmFmPnOcmaU130_provenance.