Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion description "[Werner syndrome (WS) is a progeroid syndrome caused by autosomal recessive null mutations at the WRN locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion evidence source_evidence_literature NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion SIO_000772 11186893 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion wasDerivedFrom befree-2016 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion wasGeneratedBy ECO_0000203 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- befree-2016 importedOn "2016-02-19" NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.