Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion wasGeneratedBy ECO_0000203 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion wasDerivedFrom befree-20140225 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion SIO_000772 22004887 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion evidence source_evidence_literature NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion description "[This report provide a wide spectrum of USH2A mutations and clinical features, including atypical Usher syndrome phenotypes resembling Usher syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.