Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_assertion description "[Mutations in FOXL2 gene, located in chromosome 3, are related to the development of BPES with POF (BPES type I) or without POF (BPES type II).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_assertion evidence source_evidence_literature NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_assertion SIO_000772 19969293 NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_assertion wasDerivedFrom befree-20140225 NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_assertion wasGeneratedBy ECO_0000203 NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP794432.RAh3JkKRRY97QbMfEFzyUrKw5ho2pxRlBzVmkoC8ttJKk130_provenance.