Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_assertion description "[known recessive DEB C7 mutations perturb critical functions of the C7 molecule and may have a role in dystrophic epidermolysis bullosa ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_assertion evidence source_evidence_literature NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_assertion SIO_000772 18450758 NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_assertion wasDerivedFrom lhgdn-20090331 NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_assertion wasGeneratedBy ECO_0000203 NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP150706.RACqo9Tb-ceFAZIMgjUqpuv8wFqLYDQ0SD7uLOTDfJw9w130_provenance.