Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_assertion description "[Ten novel mutations; one deletion, two frameshift mutations, and seven missense mutations were found in German patients with oculocutaneous albinism type 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_assertion evidence source_evidence_literature NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_assertion SIO_000772 14722913 NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_assertion wasDerivedFrom lhgdn-20090331 NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_assertion wasGeneratedBy ECO_0000203 NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP152560.RA55zgdQK00nqa84IeIFdX3N3jdIUB4APnzp9pjYlOmVk130_provenance.