Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_assertion description "[Data on more than 300 patients with CN collected by the Severe Chronic Neutropenia International Registry (SCNIR) since 1994 demonstrate that, independent of the CN subtype, more than 90% of patients respond to recombinant human (rHu)G-CSF with ANCs that can be maintained at approximately 1.0 x 10(9)/L.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_assertion evidence source_evidence_literature NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_assertion SIO_000772 11957189 NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_assertion wasDerivedFrom befree-2016 NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_assertion wasGeneratedBy ECO_0000203 NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.
- befree-2016 importedOn "2016-02-19" NP352170.RAjqqsnx5zrBfibxr7OntKgyqWi7tXdluqv79hhkO693o130_provenance.