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- source_evidence_literature type ECO_0000212 NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_assertion description "[Mutations in 2 of these genes were shown to cause BFNC (KCNQ3) and hereditary deafness (KCNQ4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_assertion evidence source_evidence_literature NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_assertion SIO_000772 12707061 NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_assertion wasDerivedFrom befree-2016 NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_assertion wasGeneratedBy ECO_0000203 NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.
- befree-2016 importedOn "2016-02-19" NP391754.RA5O4fEWf0ECkjwem3fVMCsBenQH4NI64vdtiJaIgwflA130_provenance.