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- source_evidence_literature type ECO_0000212 NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_assertion description "[Identification of a novel mutation in the arginine vasopressin-neurophysin II gene in familial central diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_assertion evidence source_evidence_literature NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_assertion SIO_000772 12012274 NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_assertion wasDerivedFrom befree-20150227 NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_assertion wasGeneratedBy ECO_0000203 NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257871.RAFET898g25MiRB3Pe-IckFp68R5MlXa3OxfghEV3J6Qc130_provenance.