Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_assertion description "[OPA1 gene sequencing in patients with hereditary optic neuropathies indicates that the clinical spectrum of ADOA is larger than previously thought.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_assertion evidence source_evidence_literature NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_assertion SIO_000772 19389487 NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_assertion wasDerivedFrom befree-20140225 NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_assertion wasGeneratedBy ECO_0000203 NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584236.RAGM7KXe3Q0JPe5DE-a4DD5qACgNQicUMo_qL-UJTwXlg130_provenance.