Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_assertion description "[A homozygous nucleotide change (G6395A) was found in 2 pts with Factor V deficiency/results in the replacement of an Arg by a His in position 2074, located in the Factor V C2-domain/in this domain have not previously been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_assertion evidence source_evidence_literature NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_assertion SIO_000772 11858490 NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_assertion wasDerivedFrom lhgdn-20090331 NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_assertion wasGeneratedBy ECO_0000203 NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193393.RARwLnfy-076lOOzt-c4R70_FNJMuFdmsswMZqxCvP9mk130_provenance.