Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_assertion wasGeneratedBy ECO_0000203 NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_assertion wasDerivedFrom befree-2016 NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_assertion SIO_000772 7508181 NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_assertion evidence source_evidence_literature NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.
- NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_assertion description "[Recent studies in our laboratory established genetic linkage to the type II keratin gene locus on chromosome 12q in one family with EH and identified a single amino acid mutation in keratin 1 that is responsible for the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1309389.RAns1TMk3AVb6XvZm4Z1wkvG6JWeJeuxm0UmBbPrkQD8k130_provenance.