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- source_evidence_literature type ECO_0000212 NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_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." NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_assertion evidence source_evidence_literature NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_assertion SIO_000772 11809908 NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_assertion wasDerivedFrom befree-20150227 NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_assertion wasGeneratedBy ECO_0000203 NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP798058.RAw6M591fZ31TfAfRzRK00sgvpGbEdqDOA0Bw6ohiqLPU130_provenance.