Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- befree-2016 importedOn "2016-02-19" NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_assertion wasGeneratedBy ECO_0000203 NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_assertion wasDerivedFrom befree-2016 NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_assertion SIO_000772 19860667 NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_assertion evidence source_evidence_literature NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.
- NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_assertion description "[Non-syndromic, hereditary human cataract development is linked to point mutations in the CRYAA and CRYAB genes which encode alphaA and alphaB-crystallin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771960.RAUQE3apWg-IyXYYfO5ke93-qtxGskEldbe2WaBoV_tM8130_provenance.