Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_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." NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_assertion evidence source_evidence_literature NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_assertion SIO_000772 16984240 NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_assertion wasDerivedFrom befree-20140225 NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_assertion wasGeneratedBy ECO_0000203 NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP459043.RA0vuGr0VRaFO3A884Nke76VdWQ7oBHIBoFtHQN40dY3w130_provenance.