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- source_evidence_literature type ECO_0000212 NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_assertion description "[Scapuloperoneal spinal muscular atrophy (SPSMA) and hereditary motor and sensory neuropathy type IIC (HMSN IIC, also known as HMSN2C or Charcot-Marie-Tooth disease type 2C (CMT2C)) are phenotypically heterogeneous disorders involving topographically distinct nerves and muscles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_assertion evidence source_evidence_literature NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_assertion SIO_000772 20037587 NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_assertion wasDerivedFrom befree-20150227 NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_assertion wasGeneratedBy ECO_0000203 NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.
- befree-20150227 importedOn "2015-02-27" NP935190.RAUEUzZ19PwAaG94eTAnb_OX1Cab6l4v1LMIUyPoxVG24130_provenance.