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- source_evidence_literature type ECO_0000212 NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_assertion evidence source_evidence_literature NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_assertion SIO_000772 11817654 NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_assertion wasDerivedFrom befree-20150227 NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_assertion wasGeneratedBy ECO_0000203 NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.