Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_assertion description "[A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_assertion evidence source_evidence_literature NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_assertion SIO_000772 21271662 NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_assertion wasDerivedFrom befree-2016 NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_assertion wasGeneratedBy ECO_0000203 NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.
- befree-2016 importedOn "2016-02-19" NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.