Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- befree-2016 importedOn "2016-02-19" NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_assertion wasGeneratedBy ECO_0000203 NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_assertion wasDerivedFrom befree-2016 NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_assertion SIO_000772 18950394 NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_assertion evidence source_evidence_literature NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.
- NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_assertion description "[A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699762.RAsZa-ce8mATZZKIbMQe-wyYoNv_waDKMcBBf2Dz_VP-g130_provenance.