Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_assertion description "[Furthermore, it is unknown if heterozygous germline mutations in TSC2 can produce the neurocognitive phenotype of TSC independent of epilepsy and tubers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_assertion evidence source_evidence_literature NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_assertion SIO_000772 22189265 NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_assertion wasDerivedFrom befree-2016 NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_assertion wasGeneratedBy ECO_0000203 NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.
- befree-2016 importedOn "2016-02-19" NP948437.RAGLEItIeFewJWO5ywmvu7yj-YPpQJZSbI_TF1q8oOb9M130_provenance.