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- source_evidence_literature type ECO_0000212 NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_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." NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_assertion evidence source_evidence_literature NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_assertion SIO_000772 23957197 NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_assertion wasDerivedFrom befree-20150227 NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_assertion wasGeneratedBy ECO_0000203 NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP511319.RAaKkje9sTbCAF3rCCh3O66AaSzFuwyp6ArcuK5SbFbw8130_provenance.