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- source_evidence_literature type ECO_0000212 NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_assertion description "[Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_assertion evidence source_evidence_literature NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_assertion SIO_000772 15671307 NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_assertion wasDerivedFrom befree-20150227 NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_assertion wasGeneratedBy ECO_0000203 NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954506.RAMZyTA1Ghz3aMXK__RIfFWoTJsOi9OsIKBFNn0RLrmHk130_provenance.