Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_assertion wasGeneratedBy ECO_0000203 NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_assertion wasDerivedFrom befree-20150227 NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_assertion SIO_000772 21428921 NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_assertion evidence source_evidence_literature NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.
- NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_assertion description "[Mutations in genes encoding either hamartin [TSC1 (tuberous sclerosis complex 1)] or tuberin (TSC2) result in a multisystem disorder characterized by the development of benign tumours and hamartomas in several organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759538.RAjRC0KOXp00aGrnI62eVAwgG2Q8qFGq_IEr9ywqg_Sdg130_provenance.