Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion description "[Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion evidence source_evidence_literature NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion SIO_000772 11266688 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion wasDerivedFrom befree-2016 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion wasGeneratedBy ECO_0000203 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- befree-2016 importedOn "2016-02-19" NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.