Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_assertion description "[The X-linked type of HMSN is associated with defects of the connexin 32 gene, which encodes a gap junction protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_assertion evidence source_evidence_literature NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_assertion SIO_000772 7541290 NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_assertion wasDerivedFrom befree-2016 NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_assertion wasGeneratedBy ECO_0000203 NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311614.RAdaNkQ1n2ff2xr7FHT1UQkjJU6gtwQndfDwKwGQyiz8I130_provenance.