Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_assertion description "[Our findings expand the molecular, cellular, and clinical spectrum of HPS-2 and call for an increased index of suspicion for this diagnosis among patients with features of albinism, bleeding, and neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_assertion evidence source_evidence_literature NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_assertion SIO_000772 11809908 NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_assertion wasDerivedFrom befree-2016 NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_assertion wasGeneratedBy ECO_0000203 NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.
- befree-2016 importedOn "2016-02-19" NP343198.RAGW17t6PqxKMzywldjTXS6GtFqjkUZBBLXoWjyPs1-Lk130_provenance.