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- source_evidence_literature type ECO_0000212 NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_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." NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_assertion evidence source_evidence_literature NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_assertion SIO_000772 21840926 NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_assertion wasDerivedFrom befree-20150227 NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_assertion wasGeneratedBy ECO_0000203 NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP268865.RAlzMqbl2vozdUsnbFRVXSXgAUUmcXsztPBP-c49H1O1c130_provenance.