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- source_evidence_literature type ECO_0000212 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion description "[A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion evidence source_evidence_literature NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion SIO_000772 18445675 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion wasDerivedFrom befree-20150227 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion wasGeneratedBy ECO_0000203 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.