Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_assertion evidence source_evidence_literature NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_assertion SIO_000772 15880681 NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_assertion wasDerivedFrom lhgdn-20090331 NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_assertion wasGeneratedBy ECO_0000203 NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.