Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_assertion description "[Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_assertion evidence source_evidence_literature NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_assertion SIO_000772 21359847 NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_assertion wasDerivedFrom befree-20140225 NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_assertion wasGeneratedBy ECO_0000203 NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455584.RAlwGsXTmupbzIg5skrsYj0CI9DzvAlDkB9k0sTRn29Ek130_provenance.