Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- befree-2016 importedOn "2016-02-19" NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_assertion wasGeneratedBy ECO_0000203 NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_assertion wasDerivedFrom befree-2016 NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_assertion SIO_000772 11134108 NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_assertion evidence source_evidence_literature NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.
- NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_assertion description "[The majority of familial CPHD cases are due to mutations in the pituitary transcription factor PROP1 (Prophet of Pit1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304010.RAyaq2zTz8fHrDBQ1ChuA6yvHaPIvG0fQ4OYD4YtTnCsk130_provenance.