Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_assertion description "[The absence of pathogenic mutations in VSX1, SOD1, COL4A3, and COL4A4 genes in our large number of unrelated keratoconus patients indicates that other genetic factors are involved in the development of this disorder; nevertheless, a significant correlation of a few polymorphisms indicates that there could be a link between specific polymorphisms and KC disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_assertion evidence source_evidence_literature NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_assertion SIO_000772 20664914 NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_assertion wasDerivedFrom gad-20150221 NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_assertion wasGeneratedBy ECO_0000203 NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP182420.RAjjoFNOtH5NsqugiIWLLhlqv82zL4vV0ZR2jVNik0UnE130_provenance.