Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_assertion description "[In the GHI groups, two homozygous OBSL1 mutations were also identified (height SDS -4.9 and -5.7) and two patients had hypomethylation in imprinting control region 1 in 11p15 or mUPD7 consistent with Silver-Russell syndrome (SRS) (height SDS -3.7 and -4.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_assertion evidence source_evidence_literature NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_assertion SIO_000772 25411237 NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_assertion wasDerivedFrom befree-2016 NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_assertion wasGeneratedBy ECO_0000203 NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238763.RAsn14gXFYuFmY06TFkT_49PG06gQZW4UGoHylau6qCqU130_provenance.