Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_assertion description "[Those with USH2 have moderate to severe congenital hearing loss, non-vestibular dysfunction and a later onset of RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_assertion evidence source_evidence_literature NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_assertion SIO_000772 16545802 NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_assertion wasDerivedFrom befree-20150227 NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_assertion wasGeneratedBy ECO_0000203 NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP767545.RAXYTTTSeelw8QqssrAF1cMeZEeSO4NOSPo95w0_t2AFk130_provenance.