Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion type Assertion NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_head.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion description "[Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion evidence source_evidence_literature NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion SIO_000772 18953341 NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion wasDerivedFrom lhgdn-20090331 NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion wasGeneratedBy ECO_0000203 NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.