Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_assertion wasGeneratedBy ECO_0000203 NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_assertion wasDerivedFrom befree-20150227 NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_assertion SIO_000772 21428921 NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_assertion evidence source_evidence_literature NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.
- NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_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." NP760128.RA_fuPmiu2Xbghd6mPtXidRG5AeaYrjijr6_wLtKsbj2g130_provenance.