Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_assertion description "[We had previously demonstrated that a complete loss of function in ZMPSTE24 was lethal in the neonatal period, whereas compound heterozygous mutations including one PTC and one missense mutation were associated with type B mandibuloacral dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_assertion evidence source_evidence_literature NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_assertion SIO_000772 21267004 NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_assertion wasDerivedFrom befree-20140225 NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_assertion wasGeneratedBy ECO_0000203 NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768953.RAtBxIEaTwYChsRLNfpTmhh38GsvBByZ2P40yREZTWhKo130_provenance.