Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion evidence source_evidence_literature NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion SIO_000772 14740321 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion wasDerivedFrom befree-20140225 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion wasGeneratedBy ECO_0000203 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.