Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion type Assertion NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_head.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion description "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_provenance.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion evidence source_evidence_literature NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_provenance.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion SIO_000772 22678705 NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_provenance.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion wasDerivedFrom befree-20150227 NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_provenance.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion wasGeneratedBy ECO_0000203 NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_provenance.