Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion type Assertion NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_head.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion description "[identified ACVRL1 mutations in hereditary hemorrhagic telangiectasia, including 4 unknown, and found that ACVRL1, and not ENG, mutations are predictive for liver disease]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion evidence source_evidence_literature NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion SIO_000772 18498373 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion wasDerivedFrom lhgdn-20090331 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.
- NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_assertion wasGeneratedBy ECO_0000203 NP215817.RArLDxOfbjT05t-vifgPTkBJd0BA57hv7HqXmfBB9axjI130_provenance.