Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion type Assertion NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_head.
- NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion description "[Actually it is thought that Pendred Syndrome occurs when both alleles of SLC26A4 gene are mutated; DFNB4 seems due to monoallelic mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_provenance.
- NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion evidence source_evidence_literature NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_provenance.
- NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion SIO_000772 22717225 NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_provenance.
- NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion wasDerivedFrom befree-2016 NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_provenance.
- NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_assertion wasGeneratedBy ECO_0000203 NP991627.RAaKY21nHqnhbQYtnOWwYJMKDSBn_77tTBe4pWmQKUbLo130_provenance.