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- source_evidence_literature type ECO_0000212 NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_assertion description "[Human insulin like growth factor (IGF) I deficiency is a rare disease associated with hearing loss, poor growth rates and mental retardation (ORPHA73272, OMIM608747).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_assertion evidence source_evidence_literature NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_assertion SIO_000772 23957197 NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_assertion wasDerivedFrom befree-2016 NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_assertion wasGeneratedBy ECO_0000203 NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1103530.RAiCQIlxp4dwWj7fv4JASTRHhtZXFSqV1O27aDHNdRqTk130_provenance.