Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_assertion description "[The largest homozygous region (~11 Mb) in the affected family members was mapped to chromosome 9, which harbors deafness, autosomal recessive 31 (DFNB31; a gene previously associated with Usher syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_assertion evidence source_evidence_literature NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_assertion SIO_000772 21738389 NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_assertion wasDerivedFrom befree-20140225 NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_assertion wasGeneratedBy ECO_0000203 NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717963.RAOBKVpuwnfHCtJjGcC8twAEw-OLOu-AFRHC-NcLMIkXs130_provenance.