Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_assertion description "[Routine germline MEN1 mutation testing of all cases of " classical " MEN1, familial hyperparathyroidism, and sporadic hyperparathyroidism with one other MEN1 related condition is justified by national testing services.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_assertion evidence source_evidence_literature NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_assertion SIO_000772 15635078 NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_assertion wasDerivedFrom lhgdn-20090331 NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_assertion wasGeneratedBy ECO_0000203 NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP130797.RABoWHeOW42ZZUJ7gW1OU5RiRlJ1zVaYlw-N_RI1nluqc130_provenance.