Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_assertion wasGeneratedBy ECO_0000203 NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_assertion wasDerivedFrom befree-20140225 NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_assertion SIO_000772 20083694 NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_assertion evidence source_evidence_literature NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_assertion description "[Heterozygous, loss-of-function, germline mutation in the LEMD3 gene (which encodes an inner nuclear membrane protein called LEMD3, or MAN1) has been repeatedly documented in patients with BOS or OPK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939869.RAWfeRWcF75i7oa_Z_UPNL2kOMFUq_JOzSFRvnfK1towY130_provenance.