Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_assertion wasGeneratedBy ECO_0000203 NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_assertion wasDerivedFrom befree-20140225 NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_assertion SIO_000772 9237260 NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_assertion evidence source_evidence_literature NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_assertion description "[Within 15q11-q13, four genes (SNRPN, IPW, ZNF127, FNZ127) and two expressed sequence tags (PAR1 and PAR5) have been found to be expressed only from the paternally inherited chromosome, and therefore all must be considered candidate genes involved in the pathogenesis of PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868361.RArVfm0OeRZ_8DFtlP6pote2vfMIqXRHQrC1ecfLHF7H8130_provenance.