Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_assertion evidence source_evidence_literature NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_assertion SIO_000772 14684682 NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_assertion wasDerivedFrom befree-20150227 NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_assertion wasGeneratedBy ECO_0000203 NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.