Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_assertion evidence source_evidence_literature NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_assertion SIO_000772 16752392 NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_assertion wasDerivedFrom gad-20130706 NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_assertion wasGeneratedBy ECO_0000203 NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.