Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_assertion description "[Germ-line mutation of either TSC gene leads to the development of the heritable disorder TSC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_assertion evidence source_evidence_literature NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_assertion SIO_000772 15951164 NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_assertion wasDerivedFrom befree-2016 NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_assertion wasGeneratedBy ECO_0000203 NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.
- befree-2016 importedOn "2016-02-19" NP499067.RAsr7Qcg6MXQ_2h_Nq6f71o-iLmmeDSH8HSrSiCH6eOfo130_provenance.