Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_assertion wasGeneratedBy ECO_0000203 NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_assertion wasDerivedFrom befree-20150227 NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_assertion SIO_000772 10973248 NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_assertion evidence source_evidence_literature NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.
- NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720574.RAO7VlxKuuTxK1zPxX0NKt3HEmwHxvMOgkCqwjv4LRqrw130_provenance.