Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_assertion description "[Moreover, future studies on CESD prevalence in African and Asian populations may require full-gene LIPA sequencing to determine heterozygote frequencies, since c.894G>A is not common in these racial groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_assertion evidence source_evidence_literature NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_assertion SIO_000772 23424026 NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_assertion wasDerivedFrom befree-20140225 NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_assertion wasGeneratedBy ECO_0000203 NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447691.RAU_wmwxR8iw3Sa2fn87geEt1XEKwxys62Akcgz-2VYxU130_provenance.