Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion description "[Our study illustrates that if only a single heterozygous SLC26A4/PDS mutation is found in a patient with goiter and deafness, other genetic explanations should be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion evidence source_evidence_literature NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion SIO_000772 16684826 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion wasDerivedFrom befree-2016 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion wasGeneratedBy ECO_0000203 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- befree-2016 importedOn "2016-02-19" NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.