Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_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." NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_assertion evidence source_evidence_literature NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_assertion SIO_000772 16545802 NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_assertion wasDerivedFrom befree-20140225 NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_assertion wasGeneratedBy ECO_0000203 NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435315.RANPFgRyO55r8Rt7H5XGJxzsVpIcPcrCJdMXJntUfLxIU130_provenance.