Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_assertion description "[Human insulin like growth factor (IGF) I deficiency is a rare disease associated with hearing loss, poor growth rates and mental retardation (ORPHA73272, OMIM608747).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_assertion evidence source_evidence_literature NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_assertion SIO_000772 23957197 NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_assertion wasDerivedFrom befree-20150227 NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_assertion wasGeneratedBy ECO_0000203 NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP511849.RAbUquwgZkr1hpFGeue6wTGACHb647VSEwLCD2dEfLnRc130_provenance.