Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.