Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_assertion description "[ Although more detailed functional characterizations of these polymorphisms remain to be undertaken, these polymorphic sites may be useful for identifying alleles associated with mis-splicing, additional transcript factors and, more generally, in cancer-susceptibility association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_assertion evidence source_evidence_literature NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_assertion SIO_000772 16127747 NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_assertion wasDerivedFrom gad-20130706 NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_assertion wasGeneratedBy ECO_0000203 NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52195.RAm1ykfZ_E1f62b3jLU9odztpcr3jkwtZNXDBVU8voug0130_provenance.