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- source_evidence_literature type ECO_0000212 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion description "[Autosomal recessive Meckel syndrome (OMIM 249000) (MES), first described in 1822 by Johann F. Meckel, is a major monogenic malformation syndrome with a neural tube defect leading to death of the fetus in utero or shortly after birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion evidence source_evidence_literature NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion SIO_000772 7550354 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion wasDerivedFrom befree-20140225 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion wasGeneratedBy ECO_0000203 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.