Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_assertion description "[Thus, our study supports that screening for large rearrangements should be considered to improve the genetic analysis in HHT patients with no apparent mutations in ALK1 and ENG using direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_assertion evidence source_evidence_literature NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_assertion SIO_000772 18312453 NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_assertion wasDerivedFrom befree-2016 NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_assertion wasGeneratedBy ECO_0000203 NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.
- befree-2016 importedOn "2016-02-19" NP658254.RApEJwcttInE8TVxJ2MyOHyHwZ7IDEPV7aQnh3dOKSaF0130_provenance.