Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_assertion description "[Mutations in OFD1 also cause X-linked Joubert syndrome (JBTS10) and Simpson-Golabi-Behmel syndrome type 2 (SGBS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_assertion evidence source_evidence_literature NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_assertion SIO_000772 23033313 NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_assertion wasDerivedFrom befree-20140225 NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_assertion wasGeneratedBy ECO_0000203 NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP219538.RAHI5CL0DpVI0eekul36qkkbziL6oQr_o4RtIKCpzUWOo130_provenance.