Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_assertion description "[This report emphasizes concurrently that ABCC6 may be a relevant candidate gene in some cases of GACI with no mutations in the ENPP1 gene, and that GACI may be an atypical and severe end of the vascular phenotype spectrum of PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_assertion evidence source_evidence_literature NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_assertion SIO_000772 20034067 NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_assertion wasDerivedFrom befree-2016 NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_assertion wasGeneratedBy ECO_0000203 NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.
- befree-2016 importedOn "2016-02-19" NP783611.RAOxZgYNX39nEcrhOCxlVBEEwuAtV7Wm_Kz02ALMlPVRs130_provenance.