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- source_evidence_literature type ECO_0000212 NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_assertion description "[Homozygous disruption of PCP genes in mice results in a spectrum of NTDs, including defects that affect the entire neural axis (craniorachischisis), cranial NTDs (exencephaly) and spina bifida.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_assertion evidence source_evidence_literature NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_assertion SIO_000772 21840926 NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_assertion wasDerivedFrom befree-2016 NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_assertion wasGeneratedBy ECO_0000203 NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.
- befree-2016 importedOn "2016-02-19" NP917026.RANKqoa_VUKKTnmNnEcWnPDUBAT0doTgJYF-BH273n49g130_provenance.