Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_assertion description "[The skin disease erythrokeratoderma variabilis (EKV) has been shown to be associated with mutations in GJB3 and GJB4 encoding connexin (Cx)31 and Cx30.3, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_assertion evidence source_evidence_literature NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_assertion SIO_000772 16297190 NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_assertion wasDerivedFrom befree-20140225 NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_assertion wasGeneratedBy ECO_0000203 NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP557616.RAv_bmfnTc9XZ8o-PxL2p9Lvp2gHrOcI9H5rX8GEQNgBs130_provenance.