Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_assertion wasGeneratedBy ECO_0000218 NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_assertion wasDerivedFrom uniprot-2016 NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_assertion SIO_000772 10618407 NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_assertion evidence source_evidence_curated NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.
- NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_assertion description "[A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569.RADPz5gxwUPiXXqXVITa6wy2TT5LMQrumY5ILkPOPOv7Y130_provenance.