Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_assertion description "[Mutations in the genes encoding transforming growth factor ? receptors 1 and 2 (TGFBR1 and TGFBR2) have recently been associated with hereditary connective tissue disorders with widespread vascular involvement, including arterial dissection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_assertion evidence source_evidence_literature NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_assertion SIO_000772 21270064 NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_assertion wasDerivedFrom befree-20150227 NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_assertion wasGeneratedBy ECO_0000203 NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP733884.RAsUd8fRz57v8qNvBZQHvWi2RcyR6HoVq1pZvCWjDCKhI130_provenance.