Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion type Assertion NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_head.
- NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion description "[DA type 5D (DA5D) is a rare, autosomal-recessive DA previously defined by us and is characterized by congenital contractures of the hands and feet, along with distinctive facial features, including ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_provenance.
- NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion evidence source_evidence_literature NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_provenance.
- NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion SIO_000772 23261301 NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_provenance.
- NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion wasDerivedFrom befree-2016 NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_provenance.
- NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_assertion wasGeneratedBy ECO_0000203 NP1038004.RAm8JaM3BjfHZPUgHmcsgpY3ztg9sXBa_usCcNj2N_Rds130_provenance.