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- source_evidence_literature type ECO_0000212 NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_assertion wasGeneratedBy ECO_0000203 NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_assertion wasDerivedFrom lhgdn-20090331 NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_assertion SIO_000772 14981720 NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_assertion evidence source_evidence_literature NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.
- NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_assertion description "[A daughter who carried the der Y had the clinical features of Prader-Willi syndrome while a son who carries the der 15 has mild developmental delay and hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183482.RAlS7bLzQEPcpmN1pt6P7laDLkbQSuAdRJOZchpmZLt24130_provenance.