Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_assertion description "[A combination of single-strand conformation polymorphism (SSCP) and automated DNA sequencing was used to systematically screen this gene for sequence variations in 374 unrelated probands with a clinical diagnosis of Stargardt disease, 182 patients with age-related macular degeneration (AMD), and 96 normal subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_assertion evidence source_evidence_literature NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_assertion SIO_000772 11328725 NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_assertion wasDerivedFrom gad-20150221 NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_assertion wasGeneratedBy ECO_0000203 NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP61501.RA7ec9B103b9f9CKU16lkbEkMFmmioWnM-Q71RZtCnJPw130_provenance.