Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_assertion evidence source_evidence_literature NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_assertion SIO_000772 17952667 NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_assertion wasDerivedFrom befree-20150227 NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_assertion wasGeneratedBy ECO_0000203 NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355600.RAI2kM4LhcNZFFw1fLpRtobqMuU17CltPTNATVkUdHmF4130_provenance.