Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_assertion description "[Mutations of the PROP1 gene lead to combined pituitary hormone deficiency (CPHD), which is characterized by a deficiency of GH, TSH, LH/FSH, PRL and, less frequently, ACTH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_assertion evidence source_evidence_literature NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_assertion SIO_000772 16984240 NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_assertion wasDerivedFrom befree-2016 NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_assertion wasGeneratedBy ECO_0000203 NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.
- befree-2016 importedOn "2016-02-19" NP570046.RAPG550N7Wtmgh1A53cST9QC65W0P2nNsTPrahC2y5ZL8130_provenance.