Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_assertion description "[TSC has been shown to be genetically heterogeneous, with one causative gene mapping to chromosome 9q (denoted TSC1) and at least one other gene on chromosome 16p (denoted TSC2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_assertion evidence source_evidence_literature NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_assertion SIO_000772 8990004 NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_assertion wasDerivedFrom befree-2016 NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_assertion wasGeneratedBy ECO_0000203 NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365484.RAOIgufYVkkM-ZTmQGC9jlU8lEpDzSVi4mOXRAGURwlSw130_provenance.