Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion wasGeneratedBy ECO_0000203 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion wasDerivedFrom befree-20140225 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion SIO_000772 16470787 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion evidence source_evidence_literature NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.