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- source_evidence_literature type ECO_0000212 NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_assertion description "[HPTH has been associated with a number of familial diseases, such as multiple endocrine neoplasia-type 1 (MEN1), multiple endocrine neoplasia-type2A (MEN2A), neurofibromatosis type1 (NF1) and HPTH with multiple ossifying jaw fibromas (HPT-JT Syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_assertion evidence source_evidence_literature NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_assertion SIO_000772 16299679 NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_assertion wasDerivedFrom befree-2016 NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_assertion wasGeneratedBy ECO_0000203 NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.
- befree-2016 importedOn "2016-02-19" NP523355.RAcSj4_lvcZuz-Ink0C-QIdgzU53utWbGwhyHN-xBV6uw130_provenance.