Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_assertion description "[SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_assertion evidence source_evidence_literature NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_assertion SIO_000772 15965219 NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_assertion wasDerivedFrom befree-20150227 NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_assertion wasGeneratedBy ECO_0000203 NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP847097.RAE-3jvhQbqOs3T6ZgJCdtCTC8WLtkiw-xzs0Tl-_qx_w130_provenance.