Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_assertion description "[De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_assertion evidence source_evidence_curated NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_assertion SIO_000772 22366783 NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_assertion wasDerivedFrom ctd_human-20150221 NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_assertion wasGeneratedBy ECO_0000218 NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP5738.RALWOsy5BLT5khSicfZ-RabfCdOt_6H9P7efXnivDfIvk130_provenance.