Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_assertion description "[PCDH21 spans 23 kb, consists of 17 exons, and encodes a protein that shows close phylogenetic relationship to cadherin-23 (CDH23), the protein involved in Usher syndrome type 1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_assertion evidence source_evidence_literature NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_assertion SIO_000772 16288196 NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_assertion wasDerivedFrom befree-2016 NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_assertion wasGeneratedBy ECO_0000203 NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.
- befree-2016 importedOn "2016-02-19" NP522763.RA6As3_xdGf3WWzcumIVDX-Nmq7ZgxIR5pHspBKPBndzw130_provenance.