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- source_evidence_literature type ECO_0000212 NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_assertion description "[PROP1 gene mutations lead to combined pituitary deficiency, and HESX gene mutations result in septo-optic dysplasia, both of which include HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_assertion evidence source_evidence_literature NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_assertion SIO_000772 10727999 NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_assertion wasDerivedFrom befree-20150227 NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_assertion wasGeneratedBy ECO_0000203 NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP648846.RATzQ-MfawZk_Pm7PFZjSMzkflJEyEqlnk9myI1FNtNtc130_provenance.