Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_assertion description "[Indeed, mutations in LPIN2 cause a syndromic form of chronic recurrent multifocal osteomyelitis known as Majeed syndrome, while mutations in pstpip2 cause a murine form of the disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_assertion evidence source_evidence_literature NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_assertion SIO_000772 17496555 NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_assertion wasDerivedFrom befree-20140225 NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_assertion wasGeneratedBy ECO_0000203 NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP592250.RA358smgrK3-IWt0pE4aKqAc5ho8tANYexVjra-RmP-Tg130_provenance.