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- source_evidence_literature type ECO_0000212 NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_assertion evidence source_evidence_literature NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_assertion SIO_000772 25342199 NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_assertion wasDerivedFrom befree-2016 NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_assertion wasGeneratedBy ECO_0000203 NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.