Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- befree-2016 importedOn "2016-02-19" NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_assertion wasGeneratedBy ECO_0000203 NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_assertion wasDerivedFrom befree-2016 NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_assertion SIO_000772 17704776 NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_assertion evidence source_evidence_literature NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.
- NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_assertion description "[Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625712.RAl8CMR_rJbEKUUf4mAYplt8E87ZuCubV91SCZEjF3lvk130_provenance.