Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion> ?p ?o ?g. }
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- NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion type Assertion NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_head.
- NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion description "[In this study, we investigate the occurrence of inherited deleterious variants in GALNT12 in 118 families referred to a cancer genetics clinic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_provenance.
- NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion evidence source_evidence_literature NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_provenance.
- NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion SIO_000772 22461326 NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_provenance.
- NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion wasDerivedFrom befree-20150227 NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_provenance.
- NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_assertion wasGeneratedBy ECO_0000203 NP945133.RAXNi9TU5Fwvlm8C4WkplWz-WMSDpG_HCbuWB7UiV2vtQ130_provenance.