Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion type Assertion NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_head.
- NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion description "[Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_provenance.
- NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion evidence source_evidence_curated NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_provenance.
- NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion SIO_000772 16684826 NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_provenance.
- NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion wasDerivedFrom uniprot-20150221 NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_provenance.
- NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_assertion wasGeneratedBy ECO_0000218 NP1201.RAPhQeFsjvGQTEp6Cf19TfNgk6459VC0D8pzYSZ9A-mMw130_provenance.