Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_assertion evidence source_evidence_literature NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_assertion SIO_000772 14684682 NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_assertion wasDerivedFrom befree-2016 NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_assertion wasGeneratedBy ECO_0000203 NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.