Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_assertion wasGeneratedBy ECO_0000218 NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_assertion wasDerivedFrom uniprot-2016 NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_assertion SIO_000772 17018384 NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_assertion evidence source_evidence_curated NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.
- NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_assertion description "[Type II Glanzmann thrombasthenia in a compound heterozygote for the alpha IIb gene. A novel missense mutation in exon 27.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4719.RA75lM21V-cnJdrrnc1ipmAv4MgXHp7gg2xck7PMQnYBs130_provenance.