Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_assertion description "[We screened DNA from 310 patients with normosmic IHH (nIHH) and 192 healthy control subjects for sequence changes in GNRH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_assertion evidence source_evidence_literature NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_assertion SIO_000772 19567835 NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_assertion wasDerivedFrom befree-20140225 NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_assertion wasGeneratedBy ECO_0000203 NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.
- befree-20140225 importedOn "2014-02-25" NP656002.RAndMbTKRGcuIq3YXOO6L82D0c2fST4rcG47k8joR5Tro130_provenance.