Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_assertion description "[TTR gene analysis has useful applications in genetic counselling, including prenatal diagnosis, in identifying the cause of seemingly sporadic cases of amyloid neuropathy, and in epidemiological studies of FAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_assertion evidence source_evidence_literature NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_assertion SIO_000772 2564060 NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_assertion wasDerivedFrom befree-20150227 NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_assertion wasGeneratedBy ECO_0000203 NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP310241.RAG47t-pu3DagfNjGi894JJIor1kwqrTeqfTXTGiS53Fo130_provenance.