Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_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." NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_assertion evidence source_evidence_literature NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_assertion SIO_000772 21270064 NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_assertion wasDerivedFrom befree-20140225 NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_assertion wasGeneratedBy ECO_0000203 NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP603732.RA6x7J9TT3Lor-pSzpYiaV8bQXt0_DNV--vNgdFKxNK2g130_provenance.