Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_assertion description "[We screened for mutations in ENDOGLIN(ENG), SMAD1, SMAD2, SMAD3, SMAD4, SMAD5, SMAD6 and SMAD8 genes, which are involved in the TGF-beta/BMP signallings, in 23 patients with IPAH who had no mutations in BMPR2 or ALK1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_assertion evidence source_evidence_literature NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_assertion SIO_000772 19211612 NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_assertion wasDerivedFrom befree-20140225 NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_assertion wasGeneratedBy ECO_0000203 NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212214.RALBm7SptVGQmcnoF5sqK0Flsc0F7ZEr8fhXWXNZKGrBw130_provenance.