Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_assertion description "[Deficiency of the paternal 15q11-q13 snoRNA HBII-85 locus is necessary to cause the neurodevelopmental disorder Prader-Willi syndrome (PWS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_assertion evidence source_evidence_literature NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_assertion SIO_000772 19656775 NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_assertion wasDerivedFrom befree-20140225 NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_assertion wasGeneratedBy ECO_0000203 NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP809617.RAPxVM1C0c3kBc3Ym2f9F5rtNZg4h3iFiMG_vfcANjXZc130_provenance.