Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion> ?p ?o ?g. }
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- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion type Assertion NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_head.
- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion evidence source_evidence_literature NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion SIO_000772 11817654 NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion wasDerivedFrom befree-20140225 NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion wasGeneratedBy ECO_0000203 NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.