Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_assertion description "[Six patients with the diagnosis of both complete or segmental UPD including Prader-Willi syndrome (PWS; matUPD15), Angelman syndrome (AS; patUPD15), Silver-Russell syndrome (SRS; matUPD7), Beckwith-Wiedemann syndrome (BWS; patUPD11p), pseudohypoparathyroidism (PHP; patUPD20q) and a rare chromosomal rearrangement (patUPD2p, matUPD2q), were genotyped using the GeneChip Human Mapping 10K Array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_assertion evidence source_evidence_literature NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_assertion SIO_000772 15968682 NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_assertion wasDerivedFrom befree-20150227 NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_assertion wasGeneratedBy ECO_0000203 NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP704231.RAzxFyRI2IDvZJSZKOWgkbiCeR0drxxT4qWCBlA1WTnwk130_provenance.