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- source_evidence_literature type ECO_0000212 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion description "[X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion evidence source_evidence_literature NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion SIO_000772 10219749 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion wasDerivedFrom befree-20150227 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion wasGeneratedBy ECO_0000203 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.