Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_assertion description "[Fluorescence in situ hybridization (FISH) using cosmid probes for SNRPN, D15S10, and GABRB3 for the Prader-Willi syndrome (PWS)/Angelman syndrome (AS) critical region were not present on the derived chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_assertion evidence source_evidence_literature NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_assertion SIO_000772 9128934 NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_assertion wasDerivedFrom befree-20140225 NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_assertion wasGeneratedBy ECO_0000203 NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478090.RAfRAa_TNdXJl86-LAuSRcvy9K6AUotSCjFNH-4DlYO68130_provenance.