Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion> ?p ?o ?g. }
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- NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion type Assertion NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_head.
- NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion description "[Mutations in the genes of hematopoietic growth factor receptors as a cause of congenital cytopenia, such as congenital amegakaryocytic thrombocytopenia (CAMT) or severe congenital neutropenia (CN), are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion evidence source_evidence_literature NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion SIO_000772 11458519 NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion wasDerivedFrom befree-20140225 NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_assertion wasGeneratedBy ECO_0000203 NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.