Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_assertion evidence source_evidence_literature NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_assertion SIO_000772 16982806 NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_assertion wasDerivedFrom befree-20140225 NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_assertion wasGeneratedBy ECO_0000203 NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.