Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_assertion description "[Together with previously published data showing that patients who harbor PROP1 loss-of-function mutations present a progressive decline in corticotrope function, our results support a role for PROP1 in pituitary tumor development and in the maintenance of cell lineages committed to corticotrophic differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_assertion evidence source_evidence_literature NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_assertion SIO_000772 23778486 NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_assertion wasDerivedFrom befree-20150227 NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_assertion wasGeneratedBy ECO_0000203 NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP648828.RA26A8DkGf4_vLTStQtATRUz597Q173Q-MWP-gAZZgbxc130_provenance.