Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP784299.RAFs8jUgJwMN1RZ9iUeNKIexzsQIXpHZiJWEGsSoO9tQU130_provenance.