Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_assertion description "[Novel PRPF31 and PRPH2 mutations and co-occurrence of PRPF31 and RHO mutations in Chinese patients with retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_assertion evidence source_evidence_literature NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_assertion SIO_000772 19506198 NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_assertion wasDerivedFrom befree-2016 NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_assertion wasGeneratedBy ECO_0000203 NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.
- befree-2016 importedOn "2016-02-19" NP743851.RALJZl_mUnNf9sToW6TqNp6pI7mUIDOI32bF2bDEVfeu8130_provenance.