Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion type Assertion NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_head.
- NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion wasGeneratedBy ECO_0000203 NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_provenance.
- NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion wasDerivedFrom befree-20150227 NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_provenance.
- NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion SIO_000772 14594802 NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_provenance.
- NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion evidence source_evidence_literature NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_provenance.
- NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_assertion description "[Two hereditary human leukemia syndromes are severe congenital neutropenia (SCN), caused by mutations in the gene ELA2, encoding the protease neutrophil elastase, and familial platelet disorder with acute myelogenous leukemia (AML), caused by mutations in the gene AML1, encoding the transcription factor core-binding factor alpha (CBFalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372707.RAClo49swanG-v-pfc7bUmbGY2HSLZ7Qrar0bBBd5PeMw130_provenance.