Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_assertion description "[DA type 5D (DA5D) is a rare, autosomal-recessive DA previously defined by us and is characterized by congenital contractures of the hands and feet, along with distinctive facial features, including ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_assertion evidence source_evidence_literature NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_assertion SIO_000772 23261301 NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_assertion wasDerivedFrom befree-20150227 NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_assertion wasGeneratedBy ECO_0000203 NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP823167.RAfiV-PS-PfAayrfFr7UWYcDs4XAZXHtE79k5gcV0xSBU130_provenance.