Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_assertion description "[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_assertion evidence source_evidence_literature NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_assertion SIO_000772 12920067 NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_assertion wasDerivedFrom lhgdn-20090331 NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_assertion wasGeneratedBy ECO_0000203 NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.