Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_assertion description "[We conclude that hepatic manifestation in HHT patients is associated with mutations in the ALK1 gene, but rarely with ENG mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_assertion evidence source_evidence_curated NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_assertion SIO_000772 15712270 NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_assertion wasDerivedFrom uniprot-20130724 NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_assertion wasGeneratedBy ECO_0000218 NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP182.RAPp42jmg6ybehz3IuOGg9ZC3QNHk__BLl-YJTt9xRHLg130_provenance.