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- source_evidence_literature type ECO_0000212 NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_assertion evidence source_evidence_literature NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_assertion SIO_000772 7573046 NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_assertion wasDerivedFrom befree-2016 NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_assertion wasGeneratedBy ECO_0000203 NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.