Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion description "[While these malformations are believed to result from the effects of TSC1 or TSC2 gene mutations, the molecular mechanisms leading to tuber formation, as well as the onset of seizures, remain largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion evidence source_evidence_literature NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion SIO_000772 19912235 NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion wasDerivedFrom befree-2016 NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion wasGeneratedBy ECO_0000203 NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.
- befree-2016 importedOn "2016-02-19" NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance.