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- source_evidence_literature type ECO_0000212 NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_assertion description "[A cryptic microdeletion including MBD5 occurring within the breakpoint of a reciprocal translocation between chromosomes 2 and 5 in a patient with developmental delay and obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_assertion evidence source_evidence_literature NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_assertion SIO_000772 23494922 NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_assertion wasDerivedFrom befree-20150227 NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_assertion wasGeneratedBy ECO_0000203 NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920953.RANoImslqnXCcE-LHZg8-gDBuS-9WNzygM-7u1Z8fOcxE130_provenance.