Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.