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- source_evidence_literature type ECO_0000212 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion description "[Mutations in GJB2 encoding the gap junction protein connexin-26 (Cx26) have been established as the basis of autosomal recessive non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion evidence source_evidence_literature NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion SIO_000772 9856479 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion wasDerivedFrom befree-2016 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_assertion wasGeneratedBy ECO_0000203 NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411094.RAeKWRqAk1qKeeMoCy_AwGWROA-bEnb825SKDltZs6wlU130_provenance.