Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_assertion description "[Loss-of-function mutations in the progranulin gene (PGRN) were identified in frontotemporal lobar degeneration (FTLD) with ubiquitin-immunoreactive neuronal inclusions (FTLD-U).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_assertion evidence source_evidence_literature NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_assertion SIO_000772 18565828 NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_assertion wasDerivedFrom befree-2016 NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_assertion wasGeneratedBy ECO_0000203 NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.
- befree-2016 importedOn "2016-02-19" NP677605.RAlFW6KXPYMYNrxmP1QQw5ThKlhd0IRHm4oDywFse5ZTw130_provenance.