Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_assertion description "[LAM occurs sporadically or in patients with tuberous sclerosis complex (TSC) and is etiologically linked to mutations in the TSC1 and TSC2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_assertion evidence source_evidence_literature NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_assertion SIO_000772 24570392 NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_assertion wasDerivedFrom befree-2016 NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_assertion wasGeneratedBy ECO_0000203 NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1158214.RAhTGHJJ8WITl7I8I18O32eOJUzOoMY6UHde7A-WdTonw130_provenance.