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- source_evidence_literature type ECO_0000212 NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_assertion description "[The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_assertion evidence source_evidence_literature NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_assertion SIO_000772 10982182 NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_assertion wasDerivedFrom befree-2016 NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_assertion wasGeneratedBy ECO_0000203 NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.
- befree-2016 importedOn "2016-02-19" NP294745.RA_cGQfyaP_tyMZzBmKmCPLwVdCThU7xaXhehxeF4eheI130_provenance.