Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_assertion evidence source_evidence_literature NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_assertion SIO_000772 12676894 NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_assertion wasDerivedFrom befree-20150227 NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_assertion wasGeneratedBy ECO_0000203 NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.