Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion wasGeneratedBy ECO_0000203 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion wasDerivedFrom befree-20140225 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion SIO_000772 24001744 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion evidence source_evidence_literature NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion description "[Heterozygous mutations in NPR2 could be an important cause of nonsyndromic familial short stature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.