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- source_evidence_literature type ECO_0000212 NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_assertion description "[All Task2-positive RTN neurons were lost in mice bearing a Phox2b mutation that causes the human congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_assertion evidence source_evidence_literature NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_assertion SIO_000772 20133877 NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_assertion wasDerivedFrom befree-2016 NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_assertion wasGeneratedBy ECO_0000203 NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.
- befree-2016 importedOn "2016-02-19" NP792062.RAHTn4NND-nu5_82gviQ9_FD2uTlfakQOdfpTPeEt1bng130_provenance.