Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_assertion description "[Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_assertion evidence source_evidence_literature NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_assertion SIO_000772 12114496 NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_assertion wasDerivedFrom lhgdn-20090331 NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_assertion wasGeneratedBy ECO_0000203 NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211252.RAhvUfxqbcxNrELJCU74dwdSjFstV6CXGKA4fIyA6uYVU130_provenance.