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- source_evidence_literature type ECO_0000212 NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_assertion description "[Using fluorescent connexin fusion proteins, we show that the mutation induces a transport defect similar to that found for the Vohwinkel syndrome mutation p.Asp66His.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_assertion evidence source_evidence_literature NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_assertion SIO_000772 17993581 NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_assertion wasDerivedFrom befree-2016 NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_assertion wasGeneratedBy ECO_0000203 NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.
- befree-2016 importedOn "2016-02-19" NP639683.RA7N3p2kvyZq0wvvUKCwEEjaBlrmrOE_nfZ6ZadmHrid4130_provenance.