Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_assertion description "[HMSN type II (HMSN II) or CMT2, the axonal form of CMT, is genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_assertion evidence source_evidence_literature NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_assertion SIO_000772 9595994 NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_assertion wasDerivedFrom befree-20150227 NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_assertion wasGeneratedBy ECO_0000203 NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP827246.RAR_KtD5cfgpGuueXnnIB8mgyctwuqItNMGS8Tew6jmSQ130_provenance.