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- source_evidence_literature type ECO_0000212 NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_assertion description "[ARX mutations cause a diverse spectrum of human disorders, ranging from severe brain and genital malformations to non-syndromic intellectual disability (ID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_assertion evidence source_evidence_literature NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_assertion SIO_000772 21496008 NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_assertion wasDerivedFrom befree-20150227 NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_assertion wasGeneratedBy ECO_0000203 NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978131.RAhLey_7iX5_xElxGA_Ygpdj6xKdUktYINxUEhM5KdAPw130_provenance.