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- source_evidence_literature type ECO_0000212 NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_assertion description "[We also believe that the deletion of GPR35 could be responsible for the entity brachydactyly mental retardation syndrome (OMIM #600430), which was coined based on the above minority of patients with terminal 2q37 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_assertion evidence source_evidence_literature NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_assertion SIO_000772 15521982 NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_assertion wasDerivedFrom befree-20150227 NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_assertion wasGeneratedBy ECO_0000203 NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.
- befree-20150227 importedOn "2015-02-27" NP432886.RA6uYW5yRUbBfsskb3IDKqNSN9U23K23k8NKStpMNOaio130_provenance.