Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_assertion description "[Together, these findings highlight the key role of CCDC39 and CCDC40 in PCD with axonemal disorganization and IDA loss, and these genes represent major candidates for genetic testing in families affected by this ciliary phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_assertion evidence source_evidence_literature NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_assertion SIO_000772 23255504 NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_assertion wasDerivedFrom befree-20140225 NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_assertion wasGeneratedBy ECO_0000203 NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP468546.RACfhldjZkT6Sb5Xofuh8ic0C3oHst7G7RbnUul3mRP0k130_provenance.