Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_assertion description "[A patient with a rare leukodystrophy related to lamin B1 duplication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_assertion evidence source_evidence_literature NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_assertion SIO_000772 22973660 NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_assertion wasDerivedFrom befree-20140225 NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_assertion wasGeneratedBy ECO_0000203 NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430230.RAI9dCkPcnNjvUprYzr8KRYi45MmJmKwgP5pwHZW4lT_s130_provenance.