Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- befree-2016 importedOn "2016-02-19" NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_assertion wasGeneratedBy ECO_0000203 NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_assertion wasDerivedFrom befree-2016 NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_assertion SIO_000772 10818218 NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_assertion evidence source_evidence_literature NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.
- NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_assertion description "[Our findings confirm that the molecular analysis of the FMR-1 gene is necessary in MRUC patients to achieve unequivocal diagnosis of fragile X syndrome, carrier premutation detection and for accurate genetic counseling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284416.RAPC6JcoQpJvqFd5mUQLUFPFqmSDGybpDHe9M4b05tTnc130_provenance.