Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_assertion description "[The molecular composition of DAPs was recently elucidated and mutations in two genes encoding DAPs components (CEP164/NPHP15, SCLT1) have been associated with human ciliopathies, namely nephronophthisis and orofaciodigital syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_assertion evidence source_evidence_literature NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_assertion SIO_000772 24882706 NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_assertion wasDerivedFrom befree-20150227 NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_assertion wasGeneratedBy ECO_0000203 NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP865443.RAFMi7M5h2hQ-P6TkczVVCzQ1rEjzb74AU0eN6mMvxnoY130_provenance.