Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion type Assertion NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_head.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_provenance.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion evidence source_evidence_literature NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_provenance.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion SIO_000772 20447141 NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_provenance.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion wasDerivedFrom befree-20150227 NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_provenance.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion wasGeneratedBy ECO_0000203 NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_provenance.